Based on observations, staff interviews, and facility policy review, the facility failed to ensure foods stored in one of two nourishment refrigerators (South unit) were labeled, dated when opened, and not expired. This failure placed the residents on the South unit at risk for transmission of foodborne illness.Findings include:During an observation on 01/07/26 at 1:10 PM in the South unit, the nourishment refrigerator contained:A. Three Styrofoam bowls containing applesauce or pudding. Neither were labeled or dated.B. Four plastic containers containing food leftovers that were labeled with a resident's name but were not dated.C. An open can of Coke with a straw sticking out of the opening which was uncovered, not labeled, and not dated. D. Open and 3/4-full bottle of Diet Pepsi, not labeled or dated.E. Open and 3/4-full bottle of Coke Zero, not labeled or dated.F. Open and half-full bottle of orange juice, not labeled or dated.G. Open and half-full coffee creamer, not labeled or dated. During an observation and concurrent interview on 01/08/26 at 2:30 PM, the Dietary Manager (DM) confirmed the presence of the following:A. Three Styrofoam bowls containing applesauce or pudding. Neither were labeled or dated.B. Four plastic containers containing food leftovers that were labeled with a resident's name but were not dated.C. A carton of milk which expired on 01/07/26.D. Open and 3/4-full bottle of Diet Pepsi, not labeled or dated.E. Open and 3/4-full bottle of Coke Zero, not labeled or dated.F. Open and half-full bottle of orange juice, not labeled or dated.G. Open and half-full coffee creamer, not labeled or dated.The DM stated foods in the nourishment refrigerator should be labeled with the resident's name and dated when opened or put into the refrigerator. The DM stated foods that were expired should be removed. The DM discarded the expired milk. He stated the dietary department was not involved in maintaining the nourishment refrigerators, and he would find out what department was responsible. During an interview on 01/08/26 at 2:45 PM, the DM stated the charge nurses were responsible for cleaning the nourishment refrigerators. During an interview on 01/09/26 at 9:42 AM, Licensed Practical Nurse (LPN) 7 stated the Director of Nursing (DON) was responsible for monitoring the temperatures of the nourishment refrigerators but it was a team effort to keep the foods stored in a sanitary manner. During an interview on 01/09/26 at 9:43 AM, LPN4 stated the night shift charge nurse was responsible for maintaining the nourishment refrigerators and once a week, the refrigerators were cleaned and food that were out of date were removed. During a concurrent interview on 01/09/26 at 9:48 AM, the DON stated she checked the temperatures of the nourishment refrigerators daily but did not clean them or remove expired foods. The DON stated the charge nurse was responsible for cleaning the refrigerators every Wednesday night. The MDS Coordinator (MDSC) acknowledged there was unlabeled, undated, or expired food in the South unit nourishment refrigerator and stated it had just been cleaned.Review of the facility's policy titled, Monitoring of Cooler/Freezer Temperature, dated July 2025, revealed, Refrigerated food shall be labeled, dated, and monitored so that it is used by the use by date, frozen, or discarded, whichever is applicable . Night shift supervisor/charge nurse is responsible for cleaning out all nourishment room refrigerators twice per week.
Every finding on record at Evergreen Health and Rehabilitation Center
Rome, Georgia · CCN 115720
20 findings across 9 inspections, in the inspector's own words.
Data as of , released by CMS on October 8, 2026. Source: CMS Provider Data Catalog.
The inspector’s own words from form CMS-2567, unedited, including CMS’s own spacing. Names and some dates are redacted by CMS.
Inspection of January 9, 2026
2 findingsBased on record review, staff interviews, and facility policy review, the facility failed to ensure written notice to the resident or representative of the transfer to the hospital included a statement of the appeal rights, information on how to file an appeal, and appeals contact information for two of four residents (Resident (R) 91 and R79) reviewed for hospitalization in a sample of 23 residents. This failure created the potential for a lack of understanding of appeal rights should the resident not be permitted to return or disagree with the reason for transfer, potentially causing confusion or distress upon transfer.Findings include:Review of the facility's policy titled, Transfer and Discharge, dated July 2025, revealed, The facility's transfer/discharge notice will be provided to the resident and resident's representative in a language and manner in which they can understand. The notice will include all of the following at the time it is provided:a. The specific reason and basis for transfer or discharge.b. The effective date of transfer or discharge.c. The specific location (such as the name of the new provider or description and/or address if the location is a residence) to which the resident is to be transferred or discharged .d. The phone number of the representative of the Office of the State Long-Term Care Ombudsman.The facility's policy failed to address the regulatory requirement to provide information on the right to appeal, instructions for filing an appeal, and contact information for the appeals agency.1. Review of R91's admission Record, located under the Profile tab of the electronic medical record (EMR), revealed she was admitted to the facility on [DATE] with a diagnosis of pneumonia. Review of R91's Discharge - Return Anticipated Minimum Data Set (MDS), dated [DATE] and located under the MDS tab of the EMR, revealed R91 was discharged to the hospital.Review of R91's Health Status Note, dated 09/27/25 and located in the EMR under the Progress Notes tab, revealed, Resident confused, altered mental status, O2 sat [oxygen saturation] at 78% and became nonresponsive, called ambulance, sent to [hospital] for evaluation and treatment.Review of R91's Resident Transfer Form, dated 09/27/25 and provided on paper by the Social Services Director (SSD), revealed it did not contain information addressing appeal rights, instructions for filing an appeal, or contact information for the appeals agency. 2. Review of admission Record that was located under the Profile tab of the EMR indicated she had an initial admission date of 07/09/21 with diagnoses of osteoarthritis and adult failure to thrive. Review of R79's MDS with an ARD of 12/01/24, revealed R79 was discharged from the facility with the anticipation of a readmission. The MDS indicated the resident was a short-term discharge to a hospital. Review of R79's Resident Transfer Form, dated 12/01/24, revealed R79 was sent out to [local hospital name] on 12/01/24. Review of R79's Notice of Transfer, dated 12/01/24, revealed there was no appeal information or ombudsman information provided to the resident or the residents' representative. During an interview on 01/09/26 at 9:13 AM, the SSD stated she did not provide information on appeal rights, instructions, or contact information for residents transferred to the hospital. During an interview on 01/09/26 at 9:27 AM, the SSD stated notice of appeal rights and required information was not provided to residents upon transfer to the hospital, as they were told by the appeals agency it was not required. During an interview on 01/09/26 at 11:16 AM, the Administrator stated the facility did not provide appeals information on the transfer form as they were told by the appeals agency it was not required.
Inspection of September 5, 2025
5 findingsBased on observations and staff interviews, the facility failed to ensure a safe, functional, sanitary, comfortable environment in the clean linen room, the overflow Linen Room, the Biohazard Room, and the South Hall Medication Room were maintained in an clean, orderly, and sanitary manner.Findings include:Observation on 9/3/2025 at 8:55 AM, at the nurse's station near the shower room on the South Hall revealed empty cardboard boxes along the wall. A plastic cup and scattered debris to include a cotton ball and paper were observed on the floor of the nurse's station. Between the supplement room where the nourishment refrigerator was located and the locked medication room, five boxes of opened and unopened boxes of Med Pass 2.0 and Ensure nutritional supplements were observed stacked up on the floor.On 9/3/2025 at 9:00 AM, at the request of the surveyor, Licensed Practical Nurse (LPN)8 unlocked the Medication Room. Multiple items were observed on the counter in disarray and cluttered to include a clear box with medications inside. The lid was lying on the top due to the box being over filled. The floor in the Medication Room was observed with scattered debris as well as crumbs located along and underneath the cabinets.Observation on 9/3/2025 at 9:05 AM of the Nourishment Room on the South Hall behind the nurse's station revealed the inside of the refrigerator containing nutritional supplements and other food items was in disarray and the refrigerator and freezer were observed with sticky substances, in need of cleaning. On 9/3/2025 at 10:50 AM, the Assistant Director of Nursing (ADON) was asked to accompany the surveyor to the Biohazard Room. The Maintenance Director (MD) provided entry to the Biohazard Room. Upon entry into the locked and labeled room, immediately to the left was a hopper with dark gray water standing in the bottom. The hopper was in need of cleaning as there was a black substance around the rim. The hopper was observed to wobble and was not secured to the structure. Trash and other debris was observed on the floor to the left side of the hopper with an accumulation of dirt and grime on the floor and a black substance on the baseboard. To the right of the hopper, two 1-gallon containers of a chemical, a 5-gallon bucket of floor wax, a sharps container containing sharps/needles, and a red biohazard bag containing sharps containers were observed on the floor. A wet floor sign, and a small trash container with red biohazard bags stored inside were also observed in this area. Behind the door to this room, there were 12 sharps containers stacked on the floor with sharps inside. The entire floor of this room had a buildup of a dark graying/black grime. During this observation, a room attached to the Biohazard Room was observed to be open and without a door handle. When the ADON was asked what was behind the door, she stated it was where overflow laundry was kept. The threshold between the two rooms was observed with a buildup of debris. Upon entering the room, laundry was observed on the floor. The floor of this room was observed to have a buildup of dirt and grime, grayish black in color. There were laundry racks full of laundry on both sides of the room. Although the laundry racks including sheets and towels were covered with fabric covering, the laundry was falling off the racks onto the floor. The ceiling light cover was observed to have an accumulation of dead bugs. Empty boxes were observed on the floor toward the back of the room near the door along with a black trash bag on the floor. The MD stated that there were extra hangers in the trash bag. There was a large amount of grayish black debris near the base of the door along with a large amount of cobwebs and dead bugs. There was light coming in around the exit door leading to outside that may allow the entry of bugs and pests. Observation of the clean laundry room on 9/3/2025 at 11:00 AM with the ADON, revealed laundry on the floor, some appearing dirty with brown stains. There were plastic bags of laundry on the floor, two IV (intravenous) poles were sitting on top of a plastic bag of laundry and other linen on the floor. There was a box labeled name of medical supply company turned on its side at the back of the clean laundry room among the laundry on the floor. A weighing device on its side and a dolly stored in the room near the laundry was observed on the floor. Behind the entry door, there was a brownish buildup of grime on the floor. On 9/3/2025 at 11:05 AM, the Administrator was notified about the findings in the Biohazard Room, the clean laundry, and the overflow laundry rooms. During an interview on 9/4/2025 at 10:30 AM, the Housekeeping Director (HKD1), when asked about the clean linen room, verified the condition of the clean linen room and that she took full responsibility.
Based on observations, record review, staff interviews, and review of the facility policy titled, Routine Cleaning and Disinfection, the facility failed to ensure a safe, clean, comfortable, homelike environment in the North and South hallways, resident rooms for four of 24 sampled residents (Resident (R)3, R4, R20, and R5), resident shower rooms, resident equipment for five of 24 sampled Rs (R22, R25, R24, R15, and R21), and the main dining room were maintained in a safe, clean, comfortable and clutter-free manner to create a homelike environment.Findings include:Review of the facility's policy titled Routine Cleaning and Disinfection dated 9/1/2022 states, Policy: It is the policy of this facility to ensure the provision of routine cleaning and disinfection in order to provide a safe, sanitary environment and to prevent the development and transmission of infections to the extent possible. The policy in part provides Policy Explanation and Compliance Guidelines as follows: 1. Routine cleaning and disinfection of frequently touched or visibly soiled surfaces will be performed in common areas, resident rooms and at the time of discharge.4. Routine surface cleaning and disinfection will be conducted with a detailed focus on visibly soiled surfaces and high touch areas to include, but not limited to:a. Toilet flush handlesb. Bed railsc. Tray tablesd. Call buttonse. TV remotef. Telephonesg. Toilet seatsh. Monitor control panels, touch screens, and cables. i. Resident chairsj. IV polesk. Blood Pressure cuffsl. Sink faucetsm. Light switchesn. Doorknobs and levers.12. Horizontal surfaces with infrequent hand contact (windowsills and hard surface flooring) in routine resident-care areas should be cleaned:a. On a regular basisb. When soiling and spills occurc. When a resident is discharged from the facility. 13. Cleaning of walls, blinds and window curtains will be conducted when visibly soiled. During a tour of the South and North Halls on 9/3/2025 beginning at 8:30 AM, an observation was made of the outside patio/porch area through the door on the front side of the building. Several chairs with teal-colored cushions were observed in this area. The cushions were observed with black and green matter on them, and the patio area was observed with debris in need of attention. The area at the same end of the hall as the patio/porch area was observed with dirty blinds, the windowsill and the window well contained cobwebs, dead insects, and other debris.Stop sign banners with Velcro strips used on the doorways of resident rooms throughout the North Hall were observed to be soiled in a dirty black color, approximately covering one third of the banner.The South Hall shower room was observed to have missing floor tiles and with scattered debris on the floor. The shower room was cluttered with boxes of incontinence briefs stored on the floor alongside large gray storage units. There were two bathtubs containing debris, empty boxes and boxes of trash bags stored inside. At the entrance and exit of the shower room there was an accumulation or buildup of a black substance.On 9/3/2025 at 8:53 AM, above the nurse's station on the South Hall there were four ceiling tiles with water marks, gray to black in color. One of the ceiling tiles was observed to have a large area of a black substance.Observation on 9/4/2025 at 10:10 AM with the Administrator, she viewed the ceiling tiles above the nurse's station on the South Hall. The Administrator acknowledged that the ceiling tiles were with dark discoloration. She stated that the Maintenance Director (MD) kept the tiles changed and that the discoloration was caused by air conditioner condensation on the roof.Observation on 9/3/2025 at 9:20 AM of the resident dining room revealed scattered debris on the floor of the dining room. The lower portion of the wall just inside the door on the south side of the dining room was observed with dried, scattered, brownish colored splatters in need of cleaning. The windowsills were observed with office paper hole punches sitting on the sill and scattered condiment packages of honey, ketchup, mustard, and a pink pack of Sweet Plus (a packaged sweetener). The blinds on the windows in the dining room had a heavy accumulation and buildup of grime/dust. The dining room table chairs, along the back of the seat portion and at the base of the rungs, had an accumulation of dirt/dust and grime and were in need of cleaning. The legs of the tables were observed with food splatters. Near the ice machine and kitchen dish area window, two benches were observed, one turned upside down on top of the other. The underside of the bench on top contained an old paper towel, straw papers, and a sweetener package. There was a build-up of dust and grime along the floor of the north doorway entry/exit and there were scattered dry splatters on the lower portion of the wall on the north side of the dining room.Observation of the North Hall on 9/3/2025 at 9:35 AM revealed at the entrance to R3's room, there was a white mesh banner with a stop sign in the center. The right side of the banner was observed lying on the floor and was observed to be soiled with a dark grayish to black color. R3's wheelchair was observed parked beside his/her bed and was observed with a cushion in the seat. The cushion in the seat of the wheelchair was observed with the left edge open/torn with the foam exposed. The wheelchair wheel spokes were observed to have an accumulation of dust, dirt, and food particles. The bed frame at the footboard of R3's bed was observed to have an accumulation of dust, dirt, and food particles. An empty juice cup was observed underneath the mattress on the bedframe as well as a plastic soda bottle top under the bed. The floor around the bed was observed to have an accumulation of debris to include crackers and the plastic wrapping. The resident's bedside table was observed with an empty pickle jar, a can of squirt cheese without a lid; and there were crumbs observed on the overbed table. The drawers of the bedside table were open and were observed to have a heavy accumulation of food and spillage inside both drawers. Continuing with the above observation of this room revealed that R4's overbed table was found with open snack items as well as open plastic soda bottles. There were crumbs and scattered debris observed around and underneath R4's bed.Observation of R20's bed revealed a bed control hanging on the side of the bed on the rail. The sheath to cover the wiring to the bed control had multiple exposed wires. The outlet was observed to have an electrical plug plugged into it. When the surveyor pushed the bed control for the head of the bed to go up, it would not raise. The head of the bed was flat. A urinal was observed on the bedside table that was three-fourths full of urine. The overbed table was observed with dried, brown, sticky substances on the table part. The floors around R20's bed were also observed with a buildup of dirt and grime as well as food debris. On 9/3/2025 at 9:58 AM, a white mesh banner with a red stop sign in the middle was observed on the door of R5's room. The banner was observed to be soiled with what appeared to be a reddish brownish spot near the center and the right side of the banner was soiled with a dark gray blackish coloring. On 9/3/2025 at 12:03 PM, a clear plastic bag was observed at the base of the door on the North Hall leading to the fenced covered smoking patio.On 9/3/2025 at 12:10 PM, the Maintenance Director (MD) was asked to accompany the surveyor to view R20's bed control. The bed control was shown to the MD and asked if anyone had reported an issue with the remote to him previously. The MD said it had not. The MD said that the bed could be raised using a crank and that the resident usually laid flat. The MD removed the bed control from the bed by unhooking it from the foot of the bed. Observation on 9/3/2025 at 12:24 PM revealed a housekeeping cart on the North Hall just outside room [ROOM NUMBER]. The mop head was observed sitting in the water. The water was dark gray in color.During an observation on 9/3/2025 at 12:25 PM, a mop bucket was observed on the North Hall outside of the biohazard room door. The mop head was sitting in the water. The water inside the bucket was dark gray in color.During an interview on 9/4/2025 at 10:30 AM with the Housekeeping Director (HKD1), HKD1 stated that her staff consisted of three full-time housekeepers, one floor tech, a supervisor, and an assistant. When asked about her department, she stated that the new employees were trained hands on and that she normally trained them. She explained that she had made up a five-day training program. There was a checklist for what to do from going in room to time out of room. She stated they performed this for five days to help them understand what to do. When asked about the housekeeping carts and the mop bucket and how often the cleaning solution and water was changed in the bucket, she said that the mop head was changed every day. The water in the bucket was to be changed every four rooms. When the HKD1 was asked about the boxes that were observed randomly placed along the walls, nurse's stations and the shower rooms, the housekeeping supervisor explained that Mondays were the time when they had a large number of boxes. She stated the staff put boxes outside. They were supposed to put the boxes in a fenced area but if she saw them outside, she would take them to that area.When asked about the cleaning schedule, HKD1 described a deep cleaning schedule and showed the surveyor the deep cleaning sign posted when rooms were being deep cleaned. HSKP1 stated that there were five rooms a week deep cleaned, or one a day. When asked if the deep cleaning included bed frames, HSKP1 said it did. When specifically asking about R3's room, HSKP1 showed the surveyor the schedule for August and stated R3's room would have been deep cleaned August 5, 2025. The HKD1 stated that the dining room was deep-cleaned one time a month. She stated that a floor tech came in and swept and mopped the floors daily and if they saw anything on walls, they would wipe them. HKD1 was shown the areas observed in need of cleaning in the dining room to include the walls, chairs at the rungs, blinds, and benches near the dish area. HKD1 was then asked to go to R3's room with this surveyor. The HKD1 was shown the bed frame of R3 and asked if it looked like it had been part of the deep cleaning process of R3's room. She said it did not. The housekeeping supervisor was also shown the chip bag that was observed on the resident's bedframe as well as the bedside table of the resident and the inside of the drawers. The housekeeping supervisor stated that staff did not go inside the residents' drawers without the residents' permission to clean them. On 9/5/2025 at 8:45 AM, the HKD1 provided copies of the Deep Clean checklist as well as the Daily Room Cleaning checklist that was utilized to ensure that housekeeping staff were aware of the areas designated to be cleaned. The room deep cleaning checklists included the items for cleaning: Trash (clean can also), dust all high corners, clean window [NAME] (tracks) and seal, wipe food trays and the legs, wipe entire nightstand, clean walls and doors, disinfect all knobs and switches, call light and cord cleaned. The list for deep cleaning also included sweeping and mopping under and behind everything.For daily room cleaning, the following were listed: Trash, overbed food trays, nightstands, window [NAME] (tracks) and seals, check for cobwebs, check walls and doors, disinfect call lights and light switches.Observations on 9/5/2025, beginning at 9:25 AM on both the North and South Halls of resident chairs used for mobility included:The right arm rest on R22's Broda (a chair or wheelchair that provides comfort, support, and mobility) chair was observed with multiple areas of torn vinyl. The Assistant Director of Nursing (ADON) was present during the observation and confirmed the chair was in need of repair.R23's Broda chair was observed with both arm rests torn with the vinyl in need of repair. The ADON observed the chair and confirmed that the arm rests needed to be replaced.R24's left wheelchair arm rest, at the end, was observed to have frayed vinyl. The ADON confirmed the arm rest was in need of repair. R15's blue geri chair (geriatric chairs, or geri chairs, are specialized reclining chairs for seniors who require more support or versatility than a conventional wheelchair or regular chair can provide) was observed with both armrests having torn vinyl covering exposing the foam padding underneath. Debris was also observed in the seat of the chair. Certified Nursing Assistant (CNA) 4 confirmed the chair belonged to R15. The vinyl covering on the front edge of both arm rests of R21's Broda chair was observed to be torn with foam showing. CNA4 verified the chair belonged to R21. During an interview on 9/5/2025 at 9:38 AM with the Maintenance Director, when notifying him of observations where arm rests on Broda and Geri chairs were found with torn vinyl covering, he stated he would be the one to repair those. When asked about wheelchairs and routine cleaning of those, he stated that the night shift was responsible for that cleaning. He added that if one was soiled, it would be taken care of immediately.
Based on observations, staff interviews, record review, and facility policy review, the facility failed to ensure expired insulin pens and insulin vials were removed from two of four medication carts (South Hall long and South Hall short) reviewed. In addition, the facility failed to ensure two of two medication room refrigerators (North Hall and South Hall) were locked and the schedule II lock box (containing narcotics that have a high incidence of abuse) were affixed to shelving, as required. This failure had the potential of medication diversion to residents, staff or visitors, and residents receiving ineffective medications. Findings include:Review of the facility policy titled, Medication Storage in the Facility, Expiration Dating of Medications, dated February 17, 2020, revealed, .Medications and biologicals are stored safely, securely, and properly following manufacturer's recommendations or those of the supplier.Injectable medication dispensed by pharmacy will be discarded thirty (30) days after initial dose or according to the manufacturer recommended discard date. The medication will be noted with the date the medication was initially opened.Review of the facility policy titled, Medication Storage in the Facility, Storage of Medications, dated June1, 2018 revealed,.Schedule II, III, IV, and V controlled medications are stored separately from other medications in a locked drawer or compartment designated for that purpose.All medications dispensed by the pharmacy are stored in the container with the pharmacy label.The nurse will check the expiration date of each medication before administering it.No expired medications will be administered to a resident.1. During an observation of the South Hall Medication Room on 9/3/2025 at 3:10 PM with Licensed Practical Nurse (LPN) 7 revealed the medication room refrigerator was unlocked and the narcotic lock box was inside the refrigerator and not affixed to the shelving. The locked narcotic box revealed five vials of lorazepam (a medication used to treat anxiety and agitation-a scheduled IV (four) medication) was inside. In addition, the refrigerator shelves on the door and the floor of the refrigerator were noted with debris and a yellowish sticky substance. LPN7 confirmed that the locked box was not affixed, and the refrigerator was dirty.During an observation of the North Hall Medication Room on 9/3/2025 at 3:25 PM with LPN5 revealed the medication room refrigerator was unlocked and the narcotic lock box was locked but was not affixed to the shelf in the refrigerator. The narcotic locked box contained 12 vials of lorazepam. LPN5 confirmed that the locked box inside the refrigerator was not affixed to the shelving.2. Review/observation of the South Hall Short Medication Cart on 9/4/2025 at 8:19 AM with LPN 6, who administered medications from the Short Hall cart, revealed one Lantus (long-acting insulin) kwik pen without a name, date when opened, and/or expiration date on the pen. The kwik pen showed a full vial was 260 units however, the vial showed 80 units. LPN 6 confirmed that the kwik pen did not have a resident's name on it and had been used but did not know which staff was using the unlabeled pen. LPN6 stated she did not know for certain which resident was receiving the insulin from the kwik pen but R17 was the only resident receiving Lantus from that medication cart.Review/observation of the South Hall Long Medication Cart on 9/4/2025 at 9:08 AM with LPN 8 revealed the following:1. A Tresiba insulin (long-acting insulin) kwik pen with an expiration date of 8/21/2025.2. A vial of Lantus insulin with an open date of 7/18/2025 and expiration date of 8/18/2025.3. A vial of Lispro insulin (short-acting insulin) which was not dated when opened or had an expiration date listed on the vial but had been used.4. A vial of Lispro insulin which was opened which had an open date of 7/30/2025 and an expiration date of 8/27/2025.5. There was one vial of Lantus insulin and one vial of Lispro insulin that were unopened and unused, however, the label stated that it was to be refrigerated until opened.LPN 8 stated during the observation that the insulins were expired and should not have been used. LPN 8 further stated that insulin should be refrigerated until opened.During an interview on 9/5/2025 at 9:35 AM, the Assistant Director of Nursing (ADON) stated that insulins should not be used after the expiration date and the medication room refrigerators were to be locked.
Based on observations, record review, and resident and staff interviews, the facility failed to ensure staff provided nail care for one of four residents (Resident (R) 3) observed for the provision of ADL (activities of daily living) care out of a total sample of 24 residents resulting in dirty, long, and jagged nails.Findings include:Review of the admission Record located in the electronic medical record (EMR) was admitted to this facility with diagnoses including but not limited to major depression. Review of R3's annual Minimum Data Set (MDS) with an Assessment Reference Date (ARD) of 6/20/2025 identified him as having a Brief Interview for Mental Status (BIMS) score of five out of 15, indicating R3 was severely cognitively impaired. The MDS also identified R3 as needing partial to moderate assistance with personal hygiene. Review of R3's Care Plan tab in the EMR revealed a care plan dated 7/3/2024 identifying R3's refusal for care. Nursing interventions include: Encourage resident to accept care. If refusal occurs, wait and approach at a later time. Review of the documentation in the electronic software utilized by the facility for documenting care, the task for Personal Hygiene from 5/8/2025 through 9/4/2025 was reviewed. During this time frame, documentation revealed that R3 received care and was either independent, received limited assistance, or received total assistance in the receipt of personal hygiene. The staff did not document during the 9/3/2025 to 9/4/2025 timeframe that R3 refused care for personal hygiene but did have care provided on both days.On 9/3/2025 at 9:35 AM, R3 was observed in his room in bed lying on his right side. R3's fingernails were observed to be long and jagged with a brown substance observed underneath the nails. On 9/3/2025 at 12:21 PM, R3 was asked if this surveyor could see his nails. R3 showed the surveyor his nails and the nails were in the same condition as the previous observation. On 9/4/2025 at 8:28 AM, R3 was observed coming back from breakfast. When asking about R3's clothing, R3 stated he got a bath the previous day (Tuesday) and changed his clothing.During an interview on 9/4/2025 at 3:40 PM, the Assistant Director of Nursing (ADON) provided the care plan regarding refusals for R3. While the care plan addressed refusals, it was not specific to personal hygiene or nail care. The ADON was notified that on 9/3/2025 and up to the time of this conversation, that R3's nails had been observed to be long and jagged, with brown matter underneath. The Administrator walked up to this conversation and was notified as well about R3's nails and stated staff would take care of R3's nails.
Based on observations, staff interviews, record review, and review of facility policy, the facility failed to supervise one of one (Resident (R)1) of 24 sampled residents at risk for elopement, resulting in R1 eloping from the facility. The failure had the potential to cause harm to R1 while out of the facility unaccompanied.Findings include:Review of the facility's policy titled, Elopement of Patient dated 5/10/2022 revealed the definition of elopement as occurs when a patient leaves the premises or safe area without prior authorization. Review of R1's electronic medical records (EMR) revealed that R1 was admitted to the facility with diagnoses that include but not limited to dementia with behavioral disturbance, anxiety disorder, type two diabetes, seizures, schizophrenia, and bipolar disorder.Review of the annual Minimum Data Set (MDS) with an Assessment Reference Date (ARD) of 11/26/2024 revealed a Brief Interview for Mental Status (BIMS) score of five out of 15, indicating severe cognitive impairment. Per this MDS, R1 wandered during the assessment period, and required supervision for ADL's, redirect, and supervision on and off the unit.Review of a Nursing Note in the EMR dated 11/25/2024 revealed that R1 was admitted from a family residence and was alert to self only, confused to place and time. According to this Nursing Note R1 was offered different activities but would refuse and R1's wandering occurred frequently.Review of an Elopement Evaluation completed on 11/25/2024 and located in the Assessment tab of the EMR, also identified that R1 was at risk for elopement. R1, who was able to ambulate independently without a walker or wheelchair, had risk factors including diagnosis (dementia), a history of wandering, the inability to locate significant landmarks without assistance, and attempts of routine/leisure interests that were not consistent with their new environment which could lead to exit-seeking behaviors. The Elopement Evaluation noted that the resident's behaviors included hovering near exits, as well as hyper, frustration, and restlessness and/or agitation.Review of R1's Comprehensive Care Plan, initiated on 11/25/2024, revealed R1 was care planned to prevent elopements from the day of admission. The goal for R1 to not leave the facility unattended was to be met through multiple interventions, including: Observe risk factors/triggers for exit seeking behavior and adjust care. Staff monitor [R1] frequently. [R1] photo to be in Elopement Risk book, [R1]/family member to utilize check/out logbook and Facility has exit alarms.Review of a facility document titled, Self-Reported Incident Form, dated 5/1/2025, revealed that R1 eloped from the facility on 4/30/2025. It was reported that [R1] had exited the facility unsupervised and was located off facility property. Procedures related to a missing resident were initiated and followed. During the facility search, staff were able to locate eighty-three of eighty-four residents. Charge Nurse Licensed Practical Nurse (LPN)4 notified the Administrator, local police, and family members.Observations during a tour of the facility on 9/3/2025 at 8:41 AM revealed that the secured North residential unit included one wing with resident rooms, a day area, and a central nursing station. The residential unit had four exits accessible to residents and staff, one of which led to a locked hallway, then to the main entrance. The main entrance was locked and required a code to get in and out of the facility. Two of the other locked doors led into other areas of the facility. The fourth locked side door was an exterior door opening to the parking lot. This side door was used by employees entering and exiting the facility and required a code to get in and out.Interview on 9/4/2025 at 10:10AM, the Administrator stated that there was a video tape of the incident where LPN4 opened the side door to admit Recreational Therapist (RT)1 but did not supervise R1 and R1 walked past both RT1 and LPN4, exiting the facility. This surveyor requested copies of the written facility investigation, including statements from LPN4 and RT1. The Administrator advised that written statements did not exist. A request was made to see the video tape of the incident. The Administrator stated that after ten days, the videos were recorded over, so the video of the incident no longer existed. On 9/4/2025 at 11:30AM, the Administrator and the Maintenance Director (MD) produced the video of the incident. The MD had a copy of the video in an email he sent to the police department. The video showed LPN4 opening the side door to admit RT1 and R1 walking past both, exiting the facility. The video did not contain a date stamp or a time stamp, but it did show the sun setting in the background.Interview on 9/3/2025 at 3:45PM, LPN4 stated she opened the door for RT1. [RT1] walked in as I was walking away. At no time did LPN4 see R1 exit the facility. LPN4 stated that during the medication pass around 8:00 PM that day, another staff member alerted the team that R1 could not be located. LPN4 said that all staff members did a sweep throughout the facility, and R1 could not be located. LPN4 then notified the Administrator, the Social Services Director, the police department, and the family member.Interview on 9/4/2025 at 12:45 PM by telephone, RT1 stated that around 6:30 PM or 7:00 PM he arrived at the facility and LPN4 opened the door and walked away. As LPN4 was walking away, RT1 held the door as R1 exited the facility. RT1 thought R1 was a family member that had been visiting. RT1 verified that no staff alerted him that R1 was a resident and not to let him exit.Interview on 9/3/2025 at 10:00 AM, the Social Services Director (SSD) stated that she was notified on 4/30/2025 of R1's elopement. SSD was told by the South LPN2 that R1 was found at a gasoline station by Preacher, a person known to the family of R1, near R1's nephew's apartment. R1 was taken to the nephew's apartment, but the nephew was not home. The family member of R1 was called and was told by Preacher they were taking R1 back to the facility. Around 10:00 PM on 4/30/2025, a car pulled up to the side door. R1 exited the car and was admitted to the facility. The car drove away while the police were inside the facility, along with the Administrator, the Director of Nursing, and the SSD. The SSD called the family member that evening and asked who Preacher was and how could the SSD contact him. The Family member stated that was Preacher but did not have a phone number. SSD asked again who Preacher was and the family member stated, That's Preacher.Interview with LPN2, who was the charge nurse on the South unit, on 9/3/2025 at 4:00 PM, she stated that she received a phone call on 4/30/2025 at 9:45 PM from R1's family member who stated that Preacher found R1 at a gas station near the propane tanks. R1's Family member stated that Preacher took R1 to his nephew's apartment, but no one was there. R1's Family member stated that Preacher was bringing R1 back to the facility. The Police, Administrator, SSD all see the car pull up to the side of the facility, R1 exits the car and enters the facility. The car drives away.Review of EMR under the Progress Notes dated 4/30/2025 indicate that R1 was given a thorough examination when R1 returned. There was no evidence of physical trauma or physical injury.Four attempts were made to contact the family member. No response was received.
Inspection of August 18, 2024
3 findingsBased on staff interviews, record review, and review of the facility's policies titled, Resident Assessment-Coordination with PASARR Program, the facility failed to refer one of 29 residents (R) (R61) for a pre-admission screening and resident review (PASARR) Level II screening. The deficient practice had the potential to place R61 at risk for medical complications, unmet needs, and a diminished quality of life. Findings include: Review of the policy titled Resident Assessment - Coordination with PASARR Program, dated October 2023, revealed the policy of the facility was to coordinate assessments with the preadmission screening and resident review (PASARR) program under Medicaid to ensure that individuals with a mental disorder, intellectual disability, or a related condition receive care and services in the most integrated setting appropriate to their needs. Review of the electronic medical record (EMR) revealed R61 was admitted to the facility with diagnoses including, but not limited to, anxiety disorder, major depressive disorder, and schizoaffective disorder. Review of R61's most recent entry tracking Minimum Data Set (MDS) assessment with an assessment reference date (ARD) of 7/10/2024 revealed section A (Identification Information) documented the resident had not been evaluated by Level II PASRR and determined to have a serious mental illness and/or mental retardation or related condition. Review of the quarterly MDS assessment dated [DATE] revealed Section I (Active Diagnoses) documented no neurological diagnoses and documented schizophrenia, depression, and anxiety. Review of R61's care plan revealed a focus area of mood problems related to diagnoses of depression, schizoaffective disorder, and anxiety. Goals included, but were not limited to, improved mood state. Interventions included, but were not limited to, administering medications as ordered, behavioral health consults as needed, and monitoring/recording/reporting to the medical doctor as needed for mood patterns, signs, and symptoms of depression, anxiety, or sad mood. An interview with the Social Service Director (SSD) on 8/17/2024 at 10:49 am revealed R61 did not have a PASARR Level II. She revealed that when a new diagnosis or new antipsychotic/antidepressant type medication was added to a resident's medical record, the Director of Nursing (DON) should notify her of the new psychiatric diagnosis or medication ordered, and she would submit for a PASARR Level II. She confirmed R61 had diagnoses of major depressive disorder, anxiety disorder, and schizoaffective disorder and did not have a diagnosis of dementia or Alzheimer's. She stated she was not told about the diagnosis of schizoaffective disorder and that a request for a PASARR Level II should have been submitted. An interview with the DON on 8/17/2024 at 11:04 am revealed the SSD and the MDS Coordinator meet regularly regarding psychiatric medications and diagnoses and that the MDS Coordinator should have notified the SSD of all diagnoses related to R61's mental health. An interview with the MDS/Care Plan Coordinator on 8/17/2024 at 11:06 am revealed that it was the DON's and MDS Coordinator's responsibility to notify the SSD of mental health diagnoses and new mental health medications. She stated she was unable to say why the SSD was not notified of the diagnosis of schizoaffective disorder for R61 but that she should have been notified. She stated this practice could result in R61 not receiving the specialized services he may need. An interview with the DON on 8/17/2024 at 11:50 am revealed the MDS Coordinator should communicate diagnoses to the SSD. She stated the lack of communication could cause the resident to have a mental health issue and cause the resident to be sent to the emergency room and/or hospitalized .
Based on observations, resident and staff interviews, record review, and review of the facility policy titled, Comprehensive Care Plans, the facility failed to follow the care plan related to correctly administering the physician ordered rate of oxygen (O2) for two of 15 residents (R) (R41 and R47) receiving O2 therapy. Additionally, the facility failed to follow the care plan related to cleaning the O2 filter on the O2 concentrator (machine that converts room air into oxygen) per physician's orders for two of 15 residents (R32 and R61) receiving O2 therapy. Findings include: A review of the facility policy titled Comprehensive Care Plans, implemented May 2023 revealed under Policy Explanation and Guidelines: . 8. Qualified staff were responsible for carrying out interventions specified in the care plan and will be notified of their roles and responsibilities for carrying out the interventions, initially and when changes are made. 1. A review of the manufacturer's user manual for R32's oxygen concentrator revealed the device should be operated in a clean environment, and excessive dust could affect optimal performance. If environmental conditions were less than optimal, the device would require cleaning more frequently. A review of the electronic medical record (EMR) revealed a physician's (MD) order dated 7/25/2024 revealed R32 was to receive 2 liters per minute (LPM) of oxygen (O2) via nasal cannula (NC) as needed (PRN) and to clean the O2 filter with soap and water (H2O) once a week and as needed. A review of R32's care plan revealed that the staff was to clean the O2 filter on the O2 concentrator per MD order. An observation of R32 on 8/16/2024 at 9:27 am and 8/17/2024 at 8:48 am revealed she was receiving 2 LPM of O2 via NC, per MD orders. An observation of R32's oxygen concentrator on 8/16/2024 at 9:28 am and 8/17/2024 at 9:08 am revealed that the external slats on the O2 concentrator were visibly dirty, with accumulated dust over the entire filter. An observation of the filter inside the concentrator revealed the filter had an accumulation of dust and dirt over the entire internal filter During an interview on 8/17/2024 at 9:44 am with Registered Nurse (RN) CC, he acknowledged the external slats on the O2 concentrator and internal filter on R32's O2 concentrator were dirty and had accumulated dust covering the slats and filter. RN CC confirmed he was responsible for cleaning the filter and concentrator. During an interview on 8/17/2024 at 9:45 am with the Licensed Practical Nurse (LPN DD) revealed that the treatment nurse should clean the O2 concentrators weekly. She stated the O2 tubing and humidifier bottles should be changed weekly and as needed. She revealed this should be documented on the Treatment Administration Record (TAR) for each resident. She verified the O2 concentrator's exterior vent had an accumulation of dust and dirt, and the interior filter was dirty. 47146 2. Review of R61's quarterly Minimum Data Set (MDS) assessment with an assessment reference date (ARD) of 7/15/2024 revealed in Section O (special treatments, procedures, and programs) oxygen therapy was provided to R61 while a resident. Review of R61's care plan indicated a focus of oxygen therapy, diagnosis of asthma, shortness of breath, and altered respiratory status/difficulty breathing related to chronic obstructive pulmonary disease and centrilobular emphysema. Goals included but not limited to resident will have no signs or symptoms of poor oxygen absorption, remain free of complications of asthma, and he will maintain a normal breathing pattern. Interventions included but not limited to give medications as ordered by physician (9/13/2023), give oxygen as ordered as needed (9/13/2023), monitor for signs and symptoms of respiratory distress (9/13/2023), monitor for signs / symptoms of asthma attack, and monitor, document, report breathing abnormalities to the physician (9/13/2023), and monitor/document breathing patterns, report abnormalities to the physician (9/13/2023). Review of the EMR revealed physician's orders for R61 included but was not limited to oxygen at two liters per minute via nasal cannula as needed, change oxygen tubing every week and as needed, and clean filter with soap and water every week and as needed. Review of the TAR revealed in August of 2024, change O2 tubing and concentrator cleaned was documented as refused on 8/9/2024 but documented as completed on 8/2/2024 and 8/16/2024. Review of the TAR for July 2024 revealed that the tasks change O2 tubing and concentrator cleaned was documented as completed each week. Observations made on 8/16/2024 at 11:26 am of O2 concentrator at R61's bedside revealed O2 tubing was dated 8/9/2024, the filter vent was covered with a gray substance. Observation made on 8/17/2024 at 7:45 am of the O2 concentrator at R61's bedside revealed a gray substance covered the filter vent. Observed R61 resting in bed receiving O2 at 2 LPM via NC. The NC was dated 8/16/2024. Observation and interview on 8/17/2024 at 9:45 am with LPN DD revealed the O2 concentrators should be cleaned weekly by the treatment nurse. She stated the O2 tubing and humidifier bottles should be changed weekly and as needed. She revealed this was documented on the TAR for each resident who received O2. She confirmed and verified R61's O2 concentrator's filter vent was covered with a fuzzy, gray substance. During an interview on 8/18/2024 at 12:00 pm with the Director of Nursing (DON) revealed R61's care plan included interventions to clean the O2 concentrator and filters. She stated she expected staff to follow the care plan and if a resident refused to allow staff to clean their O2 concentrator/filter they should reapproach the resident at later time. She stated if the resident continued to refuse, then the care plan should reflect this. Interview on 8/18/2024 at 12:45 pm with the Care Plan Coordinator and the MDS Coordinator revealed that the care plan was developed from the MDS assessment. They stated the care plan interventions should be added reflecting the individual needs of each resident. They stated if a resident was refusing to allow staff to change or clean their equipment, it should be added to the care plan. They stated the care plan for R61 had an intervention added to his care plan which included change tubing, clean and maintain oxygen administration equipment per facility protocol and physician orders (not dated). They stated that they were not aware R61 refused to allow staff to clean the concentrator. 46691 3. A review of R41's quarterly MDS dated [DATE], Section O (Special Treatments, Procedures, and Programs) documented that R41 received oxygen. A review of the active physician's orders revealed an order dated 11/22/2022 for O2 at 2 LPM via NC or mask PRN. A review of R41's care plan revealed a Focus area of the resident uses O2 therapy PRN related to chronic obstructive pulmonary edema (COPD). The Interventions included giving medications as ordered by the physician. A review of the medication administration record (MAR) dated August 2024 documented that O2 was administered at 3 LPM on 8/1/2024, 8/2/2024, 8/3/2024, 8/15/2204 and 8/16/2024. Observations on 8/16/2024 at 11:15 am, 8/16/2024 at 4:00 pm, and 8/17/2024 at 10:00 am revealed R41 receiving O2 via a NC with the flow-meter set at 3.5 LPM. In an interview on 8/17/2024 at 9:10 am, LPN AA confirmed R41's physician's order of O2 at 2 LPM via NC or mask PRN. During observation of R41, LPN AA verified that he was receiving O2 via an NC at 3.5 LPM. LPN AA verified that R41's care plan included a focus area of the resident using O2 therapy PRN related to COPD, and interventions included giving medications as ordered by the physician. She confirmed if the O2 was not administered at the rate ordered by the physician, the care plan was not being followed. She further stated that not following the care plan could cause adverse effects for a resident. In an interview on 8/18/2024 at 1:00 pm, LPN BB confirmed R41's care plan included administering medications as ordered and stated if the O2 was not administered as ordered, the care plan was not being followed. She stated that O2 was considered a medication. In an interview on 8/18/2024 at 1:15 pm, the DON stated she expected licensed nursing staff to follow the interventions on the resident's care plan, and if the intervention stated to administer medications as ordered, the nurse would not be following the care plan if O2 was not being administered as ordered. She stated failing to follow care plan interventions could cause adverse effects for a resident. 44960 4. Review of the EMR for R47 revealed she was admitted to the facility with diagnoses including but not limited to chronic obstructive pulmonary disease (COPD), encephalopathy, cirrhosis of the liver, diverticulosis and end stage renal disease with dialysis. The resident's most recent Minimum Data Set (MDS) dated [DATE], revealed a Brief Interview for Mental Status (BIMS) score was coded as 05, which suggests severe cognitive impairment. Review of Physician orders for R47 revealed Oxygen Therapy-Nasal Cannula at rate of two liters PRN, initiated 11/30/2023. Review of the care plan initiated on 12/19/2023 and revised on 3/26/2024 revealed that R47 had diagnosis of sleep apnea, and shortness of breath. Care plan also states order for 02 at 2 LPM via NC PRN. Observation on 8/17/2024 at 8:43 am revealed R47's O2 concentrator set on 3 LPM, being delivered via NC. Observation on 8/18/2024 at 9:20 am and 11:20 am revealed R47's O2 concentrator flow rate set at 3 LPM, being delivered via NC. Observation and interview on 8/18/2024 at 11:35 am with the Assistant Director of Nursing (ADON) confirmed that R34's O2 tank setting was on three LPM. The ADON checked R47's medical orders in the facility's EMR and confirmed that the physician order was for two LPM via NC. The ADON stated R47 had in the past adjusted the flow meter on her 02 concentrator. During an interview on 8/18/2024 at 12:10 pm, R47 stated they never adjusted the knob on the concentrator. R47 further stated only the nurses changed the flow rate on the concentrator. Interview on 8/18/2024 at 2:00 pm with the DON revealed that she expected the care plan to be reconciled with the physician's order and to be followed as written, on the care plan and physician's orders. Cross reference to F-695
Based on observations, staff interviews, record review, and review of the facility policies titled, Oxygen Administration and Oxygen Concentrator, the facility failed to ensure respiratory equipment was maintained in a sanitary manner for two of 15 residents (R) (R32 and R61) receiving oxygen therapy. In addition, the facility failed to ensure oxygen (O2) was administered according to physician orders for two of 15 residents (R41 and R47) receiving oxygen therapy. The deficient practices could potentially place the resident at risk for medical complications, unmet needs, and a diminished quality of life. Findings include: A review of the facility policy Oxygen Concentrator revised 9/1/ 2022 revealed under Policy: The staff is to follow the manufacturer's recommendations for the frequency of cleaning filters and servicing the device. A review of the facility's undated policy, copyrighted 2024, titled Oxygen Administration revealed under Policy: Oxygen is administered to residents who need it, consistent with professional standards of practice, the comprehensive person-centered care plan, and the resident's goals and preferences. The policy further stated under Policy Explanation and Compliance Guidelines: Oxygen is administered under orders of a physician, except in the case of an emergency. 1. A review of the manufacturer's user manual for R32's oxygen concentrator revealed the device should be operated in a clean environment, and excessive dust could affect optimal performance. If environmental conditions were less than optimal, the device would require cleaning more frequently. A review of the electronic medical record (EMR) revealed a physician's (MD) order dated 7/25/2024 revealed R32 was to receive 2 liters per minute (LPM) of oxygen (O2) via nasal cannula (NC) as needed (PRN) and to clean the oxygen (O2) filter with soap and water (H2O) once a week and as needed. An observation of R32 on 8/16/2024 at 9:27 am and 8/17/2024 at 8:48 am revealed she was receiving 2 LPM of O2 via NC, per MD orders. An observation of R32's oxygen concentrator on 8/16/2024 at 9:28 am and 8/17/2024 at 9:08 am revealed that the external slats on the oxygen concentrator were visibly dirty, with accumulated dust over the entire filter. An observation of the filter inside the concentrator revealed the filter had an accumulation of dust and dirt over the entire internal filter. During an interview with Licensed Practical Nurse (LPN DD) on 8/17/2024 at 9:45 am revealed that the treatment nurse should clean theO2 concentrators weekly. She stated the O2 tubing and humidifier bottles should be changed weekly and as needed. She revealed this should be documented on the Treatment Administration Record (TAR) for each resident. She verified the O2 concentrator's exterior vent had an accumulation of dust and dirt, and the interior filter was dirty. During an interview on 8/17/2024 at 9:44 am with Registered Nurse (RN) CC, he acknowledged the external slats on the O2 concentrator and internal filter on R32's O2 concentrator were dirty and had accumulated dust covering the slats and filter. RN CC confirmed he was responsible for cleaning the filter and concentrator. During an interview on 8/17/2024 at 9:50 am with the Administrator, she stated the O2 concentrator should have been cleaned weekly, and that acknowledged the exterior slats on the oxygen concentrator and the interior filer were covered with an accumulation of dust and dirt. She stated the treatment nurse cleaned the concentrators and changed the O2 tubing and humidifier bottles every week and recorded this on the TAR. 47146 2. Review of R61's quarterly Minimum Data Set (MDS) assessment with an assessment reference date (ARD) of 7/15/2024 revealed a Brief Interview for Mental Status (BIMS) of 5, which indicates R61 had severe cognitive impairment. Section O (special treatments, procedures, and programs) indicated oxygen therapy was provided to R61 while a resident. Review of R61's care plan indicated a focus of oxygen therapy, diagnosis of asthma, shortness of breath, and altered respiratory status/difficulty breathing related to chronic obstructive pulmonary disease and centrilobular emphysema. Goals included but not limited to resident will have no signs or symptoms of poor oxygen absorption, remain free of complications of asthma, and he will maintain a normal breathing pattern. Interventions included but not limited to give medications as ordered by physician (9/13/2023), give oxygen as ordered as needed (9/13/2023), monitor for signs and symptoms of respiratory distress (9/13/2023), monitor for signs / symptoms of asthma attack, and monitor, document, report breathing abnormalities to the physician (9/13/2023), and monitor/document breathing patterns, report abnormalities to the physician (9/13/2023). Review of the EMR revealed physician's orders for R61 dated 10/4/2023 for O2 @ (at) 2L/M (liters per minute/LPM) VIA NC PRN, change oxygen tubing every week and as needed, and clean filter with soap and water every week and as needed. Review of the TAR for R61 revealed in August of 2024, change oxygen tubing and concentrator cleaned was documented as refused on 8/9/2024 but documented as completed on 8/2/2024 and 8/16/2024. Review of the TAR for July 2024 revealed that the tasks change oxygen tubing and concentrator cleaned was documented as completed each week. Observations made on 8/16/2024 at 11:26 am of the O2 concentrator at R61's bedside revealed O2 tubing was dated 8/9/2024, and the filter vent was covered with a gray substance. Observation made on 8/17/2024 at 7:45 am of the O2 concentrator at R61's bedside revealed a gray substance covered the filter vent. R61was observed resting in bed receiving O2 at two LPM via NC. The NC was dated 8/16/2024. Observation and interview on 8/17/2024 at 9:45 am, she confirmed and verified R61's O2 concentrator's filter vent was covered with a fuzzy, gray substance. During an interview on 8/18/2024 at 1:33 pm with RN CC revealed he did not remember R61 refusing to allow him to change oxygen tubing or clean his O2 concentrator. He stated when R61 refused, he typically reapproached at a later time to attempt to complete the task. He stated he also would complete this task when R61went out to smoke. He stated that if he was able to complete the task after the resident previously refused, he would/should document the task was completed but also revealed that the EMR was sometimes frustrating because it didn't load in a timely manner and he may have forgotten to complete the task. 46691 3. A review of R41's quarterly MDS, dated [DATE], revealed section C (Cognitive Patterns) revealed a Brief Interview for Mental Status (BIMS) of 5 (indicating severe cognitive impairment) and section O (Special Treatments, Procedures, and Programs) documented that R41 received oxygen. A review of the active physician's orders revealed an order dated 11/22/2022 for O2 at 2 LPM via NC or mask PRN. A review of R41's diagnoses list revealed diagnoses included chronic obstructive pulmonary edema (COPD) and respiratory failure. A review of the MARs dated 8/2024 documented that O2 was administered at 3 LPM on 8/1/2024, 8/2/2024, 8/3/2024, 8/15/2204 and 8/16/2024. A review of the Progress Notes revealed no documentation of respiratory distress. Observations on 8/16/2024 at 11:15 am, 8/16/2024 at 4:00 pm, and 8/17/2024 at 10:00 am revealed R41 receiving O2 via a NC with the flow-meter set at 3.5 LPM. In an interview on 8/16/2024 at 4:00 pm, R41 stated he used the O2 as he felt he needed it, and the staff set the flow rate for him. He stated he did not adjust the settings. In an interview on 8/17/2024 at 9:10 am, LPN AA stated the nurses were responsible for ensuring residents received medications, including O2, as ordered by the physician. She stated nurses should check the physician's order each shift to ensure the O2 was being administered according to the physician's order. LPN AA confirmed R41's physician's order for O2 at 2 LPM via NC or mask PRN. During observation of R41, LPN AA verified that he was receiving O2 via an NC at 3.5 LPM. She stated she was unsure why R41's O2 was set to deliver 3.5 LPM and further stated since R41 had COPD, he could have adverse effects from receiving too much O2, and the flow meter should be monitored at least every shift to ensure O2 was administered as ordered. In an interview on 8/18/2024 at 1:15 pm, the DON stated she expected licensed nursing staff to administer O2 as ordered by the physician. She further stated the nurse should notify the physician if a resident experienced respiratory distress and should not adjust the O2 flow rate without a physician's order. She stated administering O2 at a rate higher than the ordered rate could cause adverse health effects for the resident. 44960 4. Review of the EMR for R47 revealed she was admitted to the facility with diagnoses including but not limited to chronic obstructive pulmonary disease (COPD), encephalopathy, cirrhosis of the liver, diverticulosis and end stage renal disease with dialysis. The resident's most recent MDS dated [DATE] revealed a BIMS score was coded as 05, which suggests severe cognitive impairment. Review of Physician orders for R47 revealed an order for O2 @ 2L/M (LPM) VIA NC PRN, initiated 11/30/2023. Review of the care plan initiated on 12/19/2023 and revised on 3/26/2024 revealed that R47 has diagnosis of sleep apnea, and shortness of breath. Observation on 8/17/2024 at 8:43 am revealed R47's O2 concentrator set on 3 LPM being delivered via NC. Observation on 8/18/2024 at 9:20 am and 11:20 am revealed R47's O2 concentrator flow rate set at 3 LPM, being delivered via NC. Observation and interview on 8/18/2024 at 11:35 with the Assistant Director of Nursing (ADON) confirmed that R47's O2 tank setting was set on 3 LPM. ADON checked R47's medical orders in the facility's EMR and confirmed that the physician order was for two LPM via NC. During an interview on 8/18/2024 at 12:10 pm, R47 stated she never adjusts the knob on the concentrator. R47 further stated only the nurses change the flow rate on the concentrator, and that she only adjusts her tubing.
Inspection of June 21, 2023
1 findingBased on staff interviews, record review, and review of the facility's policy titled, Abuse, Neglect and Exploitation, the facility failed to protect the resident's right to be free from physical abuse by another resident, and to report an incident of alleged abuse within two hours to the state agency for one of three (R) (R#1) sampled residents reviewed for abuse. Findings include: Review of the facility's policy titled, Abuse, Neglect and Exploitation implemented on 4/01/2023, indicated Reporting of all alleged violations to the Administrator, state agency, adult protective services and to all other required agencies (e.g. [for example], law enforcement when applicable) within specified timeframes: a. Immediately, but no later than 2 hours after the allegation is made, if the events that cause the allegation involve abuse or result in serious bodily injury. Review of Admission Record for R#1 revealed the resident was admitted with diagnoses that included cerebral palsy, epilepsy, and unspecified intellectual disabilities. Review of the quarterly Minimum Data Set (MDS) with an Assessment Reference Date (ARD) of 3/21/2023 revealed R#1 had a Staff Assessment for Mental Status (SAMS) which indicated the resident had severely impaired cognitive skills for daily decision making. Review of a document titled, Facility Incident Report Form, dated 5/16/2023 indicated an incident of resident-to-resident abuse was reported by a certified nursing assistant (CNA). The CNA reported that R#2 touched R#1 inappropriately. The report indicated the incident occurred at 8:00 p.m. on 5/15/2023. There was no injury or treatment required and the physician was notified. The document indicated the state survey agency was notified of the abuse allegation on 5/16/2023 at 2:49 p.m. Review of a handwritten document from Certified Nursing Assistant (CNA) #3 addressed to the Administrator and Licensed Practical Nurse (LPN) #4 indicated CNA#3 witnessed R#2 assaulting R#1, R#2's roommate. The statement indicated that it was at approximately 6:10 p.m. on 5/14/2023 that CNA#3 witnessed R#2 with one hand on R#1's back, and with the other hand/fingers at R#1's buttocks area with the hand moving back and forth in and out of R#1's buttocks area. Interview on 6/21/2023 at 1:50 p.m. with CNA#3 revealed she did not recall the exact date or day, but as she did room checks she saw something unusual when she passed by R#2's room, so she stopped in the hall. She stated R#2 had some type of a rag in their hand and held the side rail of R#1's bed. Per CNA#3, R#2's hands were behind R#1's buttocks. CNA#3 stated she asked R#2 what they were doing, and R#2 looked at her, got up, and went to their side of the room where their bed was but did not respond. CNA#3 stated she left to get another CNA who was close by to stay in the resident room while she left to get the charge nurse to come and see what was going on. CNA#3 thought it was unusual to see R#2 next to R#1's bed but was not sure what was going on and wanted the nurse to assess the residents. CNA#3 did not see R#1 in any type of distress or yelling out or in any danger. CNA#3 stated she did not tell the nurse the resident was being abused or assaulted, but described to the nurse what she saw, stating it was not her place to make that judgement. CNA#3 stated LPN#2 told her not to do anything and that LPN#2 would call the nurse supervisor. CNA#3 thought LPN#2 called LPN#1. She stated they separated the two residents to different rooms, and CNA#3 asked both residents if they were okay. CNA#3 stated she wrote a statement and handed it to the Director of Nursing (DON) to give to the Administrator the next morning. Interview on 6/21/2023 at 2:29 p.m. with LPN#1 revealed the incident with R#1 occurred on Monday night 5/15/2023. LPN #1 reported that when LPN#2 called her the night of the incident, LPN#2 told her that CNA#3 had called LPN#2 to R#1's room but LPN#2 told her all she saw was R#1 in their bed with feces on them and R#2 in their bed wiping their hands with a washcloth because they also had feces on their hands. Per LPN#1, the staff discussed room availability so R#2 could be moved. LPN#1 stated that no one brought up any allegation of abuse until the next morning when CNA#3 gave her written statement to the DON and then it was given to the Administrator when the Administrator arrived. According to LPN#1, once the Administrator read the statement, the investigation of abuse was started. LPN#1 stated LPN#2 only told her that R#2 had gotten into feces. LPN#1 stated LPN#2 did not tell her that there was some suspicion of abuse or that they suspected R#2 may have had their fingers in R#1's rectum. LPN#1 said she would have reported it to the state agency within two hours if she had been notified of the abuse allegation earlier. Interview on 6/21/2023 at 3:15 p.m. with LPN#2 revealed the incident occurred on Monday evening, 5/15/2023. She stated CNA#3 told her she had seen R#2 kneeling next to R#1's bed and that R#2's hands were behind R#1's buttocks, and R#2 was making a back-and-forth motion with their hand near R#1's buttocks. When LPN#2 arrived at the resident room, R#2 had already stood up and was wiping their hands with a washcloth on their side of the room. LPN#2 stated she called LPN#1 immediately and reported that CNA#3 observed what she thought was R#2 with their hand/fingers on R#1's buttocks moving in a back-and-forth motion. R2's hands were covered in feces, and R#1 was covered in feces. LPN#2 reiterated that she told LPN#1 that they suspected R#2 had their fingers in R#1's rectum. LPN#2 stated LPN#1 told her to hold on while LPN#1 called the Administrator. LPN#2 stated they continued to monitor both residents during this time. When LPN#1 called LPN#2 back, she asked LPN#2 to move R#2 to another room, so they prepared to move R#2 into a new room. Interview on 6/21/2023 at 12:25 p.m. with the Administrator revealed she did not learn of the allegation of abuse until the following day on 5/16/2023 when she received a witness statement from the CNA who made the allegation of abuse. The Administrator stated she had been contacted the night before on 5/15/2023 by LPN#1 regarding an incident with R#1 and R#2 but LPN#1 told her that R#1 had a bowl movement and they found R#1 covered in feces and R#2 with soiled hands with feces. The Administrator stated they discussed room availability so they could move R#2 out of the room the two residents shared so that R#2 could not get into feces. Per the Administrator, there was no indication from the call that anyone suspected abuse. The Administrator indicated both residents had been in the facility a long while and had never had any abuse concerns. The Administrator stated as soon as she received the witness statement the next day, she realized the incident described in the statement was different than what she had been told over the phone the evening before, so she immediately reported the allegation to the state agency, notified the police, and began an investigation.
Inspection of November 10, 2020
1 findingBased on observations, interviews, and policy review, the facility failed to ensure proper cleaning and disinfecting of the Coronavirus 19 (COVID-19)/Patient Under Investigation (PUI) Unit. In one of three units (COVID-19/PUI Unit) the nursing staff were using disinfectant products prior to cleaning surfaces and were not knowledgeable of the disinfecting products contact times. Findings include: Review of the facility's undated infection control policy titled, Coronavirus (COVID-19) Policy and Procedure, under section Environmental Cleaning revealed .l. The infection preventionist and the director of environmental services have established procedures for environmental cleaning based on current CDC recommendations 2. Standard cleaning and disinfection procedures (e.g., using cleaners in water to preclean surfaces prior to applying disinfectants to frequently touched surfaces or objects or indicated contact times.) will be used for Coronavirus environmental control in all settings with in the facility including those resident care areas in which aerosol generating procedures are performed . Review of the facility's adopted Center for Disease Control (CDC) COVID-19 Policy and Procedure titled, Preparing for COVID-19 in Nursing Homes Infection Control for Nursing Homes, dated June 25, 2020, section Guidelines for cleaning and disinfection for [DIAGNOSES REDACTED] CoV 2 revealed .Clean the surface first and then apply the disinfectant as instructed. Ensure adequate contact time for effective disinfectant . Review of the facility's staff in-service titled, COVID 19 Info, Care of Resident, Space and Cleaning of Residents Rooms, dated 10/30/20, revealed an undated instructional form titled, Cleaning and Disinfecting Your Facility. The form instructed staff to clean surfaces with soap and water prior to the use of disinfectant products. Observation of the COVID 19/PUI Unit on 11/10/20 at 12:00 PM revealed the unit was clean and clutter free. There were no foul odors. The unit had two working air purifiers located on each side of the hallway. Interview with Certified Nursing Assistant (CNA) AA who was designated to work the COVID 19 unit on 11/10/20 at 12:30 PM revealed she was responsible for the cleaning and disinfecting on the unit because the housekeepers were not to come on the unit. She stated she cleaned with Sani-wipes or bleach wipes. She stated the contact times for the products she cleaned with were 20 to 30 minutes. She stated she was provided with education and training by the Director of Nursing (DON) on how to clean and disinfect the unit and what product to use. Interview with the DON on 11/10/20 at 1:00 PM revealed she had provided education and training for the CNAs regarding the cleaning and disinfecting of the COVID-19/PUI Unit. She stated she believed bleach wipes were to be used to clean the unit. A second interview with CNA AA on 11/10/20 at 1:17 PM on the COVID/PUI Unit revealed she stated she wiped everything down with the bleach or the Sani-wipes. Interview with CNA BB on 11/10/20 at 2:18 PM revealed she worked the COVID 19/PUI Unit routinely and was one of the designated CNAs to clean and disinfect the unit. She stated she was provided with education and training by the DON and Administrator on how to clean and what products to use. She stated the contact time for the bleach and Sani-wipes were three to four minutes. She stated the contact time was the time the product needed to dry on the surface. Interview with Licensed Practical Nurse (LPN) CC on 11/10/20 at 2:20 PM revealed the CNAs were responsible for cleaning and disinfecting the unit. She stated she had attended an education and training provided by the DON on cleaning of the unit and what products to use. She stated the cleaning was completed each shift daily and when needed. She stated the products used were bleach and Sani-wipes (orange top) and the contact times were four minutes. She stated the reason the contact times were important was to effectively kill the germs and to not cross contaminate. Interview with the Administrator on 11/10/20 at 4:30 PM revealed staff for the COVID-19/PUI Unit were provided education and training with demonstration and re-demonstration on how to clean surfaces and when to clean and disinfect surfaces on the unit. She stated the staff were not given instruction to wash with soap and water prior to applying the disinfectant product. She stated the contact times were discussed in the education and training. Interview with CNA DD from the second shift on 11/10/20 at 4:47 PM revealed he was provided education and training by the DON on cleaning and disinfecting the COVID-19/PUI Unit. He stated he used the bleach wipes for cleaning and the contact time was two hours. He stated contact time was the time the product needed to fully dry. Interview with the Infection Control Practitioner (ICP) on 11/10/20 at 3:00 PM revealed he was unaware the Sani-wipe contact time was three minutes and not one minute as first referenced. Review of the Environmental Protection Agency (EPA) Sani-wipe information sheets verified the contact time as three minutes.
Inspection of September 6, 2019
4 findingsBased on observations, staff interviews and review of kitchen cleaning schedules, the facility failed to label and date six packages of unsealed food items in the freezer. In addition, the facility failed to maintain the 10 loaf bread crates and the loaf bread storage cart in a clean and sanitary manner. The facility census was 93 residents. Findings include: 1. The initial observation of the kitchen with the Dietary Service Manager (DSM) on 9/3/19 which began at 10:25 a.m. revealed unsealed, undated food items in the kitchen which included two bags of hamburger patties, one package of whipped cream, one bag of okra, one bag of biscuits, and one bag of French fries. During an interview with the DSM on 9/3/19 at 10:35 a.m., he stated he was unaware of the unlabeled items in the freezer and discarded them immediately. He stated he provided education to his kitchen staff related to dating unsealed food items but was unable to provide documentation to confirm the inservice. In addition, when asked, he provided no policies and procedures related to the kitchen. Review of the Georgia Department of Public Health Food Service Establishment Inspection Report dated 3/14/19 revealed a score of 90 with a grade of [NAME] The deficient practice was described as, Several packages of unsealed deli meats not dated once opened. These items were discarded, and the deficiency was a new violation. 2. Further observation of the kitchen on 9/3/19 revealed a loaf bread storage cart with 10 loaf bread crates which were visibly soiled with a gray/black substance. When asked when the cart and crates were cleaned last, the DSM stated they had never been cleaned. Review of the Cleaning Checklists dated 6/3/19 through 9/1/19 revealed the loaf bread storage cart and crates were not listed as items scheduled for cleaning. A follow-up observation of the kitchen on 9/5/19 at 11:45 a.m., revealed the loaf bread storage cart and crates remained soiled. During an interview with the Administrator on 9/6/19 at 5:00 p.m., she stated she was unaware of the condition of the loaf bread cart and crates and would ask the Maintenance Director and the DSM to power wash them immediately. She stated her expectation was for all staff to perform their assigned duties as ordered and/or scheduled and fulfill other duties as assigned.
Based on observation, interviews and record reviews the facility failed to refer one of two Residents (R) #84 to the appropriate state-designated authority for a Level II PASARR (Pre-Admission Screening and Resident Review) screening for evaluation and determination of specialized services. Findings include: A review of an undated policy titled 'Admission Criteria' on page nine, number nine; revealed the following: All new admissions and readmissions are screened for mental disorders (MD), intellectual disabilities (ID) or related disorders (RD) per the Medicaid Pre-Admission Screening and Resident Review (PASARR) process. a. The facility conducts a Level I PASARR screen for all potential admissions, regardless of payer source, to determine if the individual meets the criteria for a MD, ID or RD b. If the level I screen indicates that the individual may meet the criteria for a MD, ID or RD, he or she is referred to the state PASARR representative for the level II (evaluation and determination) screening process. (1) the admitting nurse notifies the social services department when a resident is identified as having a possible (or evident) MD, ID or RD. (2) the social worker is responsible for making referrals to the appropriate state-designated authority c. Upon completion of the Level II evaluation, the State PASARR representative determines if the individual has a physical or mental condition, what specialized or rehabilitative services he or she needs, and whether placement in the facility is appropriate. d. The State PASARR representative provides a copy of the report to the facility. e. The interdisciplinary team determines whether the facility is capable of meeting the needs and services of the potential resident that are outlined in the evaluation. f. Once a decision is made, the State PASARR representative, the potential resident and his or her representative are notified A review of the Resident #84's (R#84) Level 1 PASARR revealed no indication of mental illness. A review of the 'Cumulative [DIAGNOSES REDACTED]. A review of R#84's medications include: Donepezil-5mg Q-day; Memantine-5mg BID; [MEDICATION NAME]-100mg @ HS; [MEDICATION NAME]-25mg Q HS; [MEDICATION NAME]; [MEDICATION NAME]; [MEDICATION NAME] Consta-25mg Injection [MEDICATION NAME] days - last received on 9/2/19. Behavior monitoring sheets for June, (MONTH) and (MONTH) 2019 revealed behaviors noted on four occasions that included resisting care; calling 911 twice and believing that someone is putting something in her food. A review of the Minimum Data Set ((MDS) dated [DATE] document a Brief Interview for Mental Status (BIMS) summary score of one (1) and indicated inattention and disorganized thinking in Section C1310. This MDS also documented Section E0100-B for delusions. A review of R#84's Care Plan, which was initiated on 3/11/19 and last reviewed on 8/20/10, revealed the resident is care planned for mood problems related to [DIAGNOSES REDACTED]. A Nurse note dated 7/24/19 revealed the following: resident noted refusing meds, cheeking meds, continues to have increased behaviors. MD notified. N.O. (new order) received, [MEDICATION NAME] 25mg IM now and Q 10 days. Family notified. left message to call back. Will continue to observe. A Nurse Note dated 8/23/19 revealed the following: Psych PAR: resident remains on [MEDICATION NAME] 100mg PO Q HS [MEDICATION NAME] 25mg PO BID; [MEDICATION NAME] PO Q HS;[MEDICATION NAME]/mL Q 10 days IM; [MEDICATION NAME] 15 mg PO Q HS [MEDICATION NAME]; XR 150mg PO QD resident has had increased behaviors, including cheeking medications, yelling at staff and calling 911; managed with 1:1, redirection, rest and meds. Will Observe. A review of the Care Plan Notes For PAR-PSYCH on 8/26/19 revealed a discussion of [MEDICATION NAME] 100mg PO Q HS; [MEDICATION NAME] 25mg PO BID. [MEDICATION NAME][MEDICATION NAME]/mL IM Q 10 days; [MEDICATION NAME] 15mg PO QHS; [MEDICATION NAME] XR 150mg PO QD; Resident has increased behaviors, yelling at staff, calling 911. Resident was managed with 1:1, redirection, rest, medications, staff will observe. During an interview with the Social Services Director (SSD) on 9/6/19 at 3:28 p.m., she reported that R#84 was admitted from a psychiatric behavioral hospital with a level 1 PASARR, that did not trigger the resident for a level II screening. During an interview with the Director of Nursing (DON) and the Patient Care Coordinator (PCC) on 9/6/19 at 3:54 p.m., the DON and PCC described the facility process for identifying and referring residents for a Level II evaluation/screening. The DON reported there are certain [DIAGNOSES REDACTED]. The Patient Care Coordinator reported, if a resident has a [DIAGNOSES REDACTED]. During the duration of the survey, no displays of yelling, cheeking medications, physical and verbally abusive behavior or agitation were observed.
Based on observations, interviews and record review, and policy review dated (MONTH) 2008 entitled Resident Assessment Management System the facility failed to follow the care plan related to the use of a positioning wedge while the resident is in bed, and a pillow behind the knee for one of one Residents (R) #13 reviewed. Findings include: A review of policy titled Resident Assessment Management System-VII-Comprehensive Care Plan dated (MONTH) 2008 revealed under A-POLICY: It is the policy of this facility to develop, in conjunction with the resident and/or representative, the Comprehensive Resident Care Plan. The Plan is directed toward achieving and maintaining optimal status of health, function and quality of life. It is completed no later than seven (7) days after the completion of the RAI. It is reviewed and revised by the Interdisciplinary Team in quarterly conferences following completion of the MDS assessment and following assessment for significant change. A review of section B, item 9 revealed; The individualized Care Plan is accessible to all caregivers to assure informed, consistent delivery of service. A review of R#13's [DIAGNOSES REDACTED]. R#13 is a left above the knee [MEDICAL CONDITION] (L-AKA). A review of section M of the MDS dated [DATE] revealed one Stage 2 pressure ulcer. A review of physician orders [REDACTED]. A review R#13's treatment orders include; 7/29/2019-med honey to bottom of right foot-open area; 7/29/2019-med honey to right heel-open area, 7/29/2019-skin prep to right 4th toe-scab. A review of the resident's treatment administration record (TAR) revealed a stage II wound to the bottom of his right foot. Other wounds noted in the documentation have healed. A review of R#13's person centered comprehensive care plan updated on 6/25/19 revealed the resident is at risk for further pressure ulcers related to incontinence, poor mobility and history of pressure ulcers. 1/21/19 unstageable right heel; 2/11/10 Stage II right 4th toe; 8/9 19 Stage II right heel; 8/9/10 stage II bottom of right foot. Interventions included; Apply pillow behind knee, and Use Wedge in bed to aid in turning. A review of the care plan notes for Patient At Risk (PAR) Wounds, revealed a note dated 5/3/19 - Unstageable to right heel is healed per the physician, Stage II to right 4th toe 0.8x0.9 cm no odor, moderate amount serous drainage, wound bed red/pink with pink attached open edges. Followed by wound physician weekly. Pressure relieving interventions in place. Continue treatment, continue to observe. A review of R#13 Resident Status Sheet in the certified nurse assistant's Activities of Daily Living (ADL) Book revealed under the special equipment category; the resident is 'total care' and 'wedge in bed.' During observations of R#13, no pillow was observed behind the knee and no wedge was used for positioning on 09/04/19 at 3:25 p.m. and 9/6/19 at 8:30 a.m. During a continuous observation of R#13 on 9/06/19 from 09:44 a.m. to 10:20 a.m. resident was in the bed with no pillow noted behind the knee or wedge in the bed. During an observation on 9/06/19 at 10:20 a.m. of employee Licensed Practical Nurse (LPN) FF and the Patient Care Coordinator (PCC) RN performing the treatment on R#13's foot, both facility employee LPN-FF and PCC agreed that the pillow that should be behind the knee and a wedge should be in the bed for positioning. During an interview on 9/04/19 at 03:43 p.m. with Certified Nursing Assistant (CNA) DD, she reported that R#13 is total care and has dementia. She indicated that she turns him following the turning schedule and changes him. She reported that if there are any special needs with a resident that the nurse will tell her. She reports that how he is right now is normal for him and that she is not aware of any special needs. During an interview on 9/06/19 at 10:42 a.m. with CNA-EE she reported that she keeps R#13 turned and feet propped up and that she places a pillow up under his leg in the chair. She reported LPN-FF or a nurse will share information about a resident's special needs. She reported she was not aware of a pillow and wedge while he is in bed. During an interview on 9/06/19 at 11:21 a.m. with LPN/Charge Nurse-CC, she reported that she is aware of resident special needs through observation and report from supervisors. She reported there is a 24-hour report book and that the nurses will share with CNAs any information they need to be aware of. She indicated for positioning or pressure relieving needs, she would ask the therapy department. She indicated that they would know about a resident position/pressure relief through the outgoing nurse. She reports that she can go to the care plan if she needs to know anything. She reports the CNAs will come to her if they need to know anything, or she will tell them anything they need to know. She reported she was not aware the resident was care planned for use of positioning items of pillow and wedge while in the bed. During an interview on 9/06/19 at 11:42 a.m. with LPN-FF, he reported that if a resident has any special needs he will tell the staff member assigned to that resident and the charge nurse. He indicated that the charge nurse will relay information to the staff.
Based on observations, review of the facility policy titled Blood Glucose Monitoring System Disinfection, and staff interview, the facility failed to ensure proper sanitization/cleaning of monitors for testing of blood sugar glucose during two of five observations, for residents (R), (R#68, R#49) on one of three halls, out of a total of 36 residents who receive glucose testing. Findings include: A review of the facility policy titled Blood Glucose Monitoring System Disinfection, dated 2011, indicated the blood glucose monitoring system will be disinfected between use of each resident to prevent transmission of infection, decrease bacterial growth and provide sanitary equipment. Item number six under Procedure indicates glucometers are cleaned with bleach germicidal wipes for five (5) minutes. An observation (by surveyor # ) of point-of-care testing for blood glucose on 9/6/19 at 11:35 a.m. with Licensed Practical Nurse (LPN) AA, revealed she failed to clean the glucometer device as directed by facility policy between two residents; On 9/6/19 at 11:35 a.m. LPN AA, opened her cart for the South hall and retrieved a small plastic box with a flip top. She opened the box to reveal a glucometer device, cotton swabs, alcohol pads, and lancets. She retrieved gloves from the top of the cart and proceeded to room [ROOM NUMBER]B, Resident (R)#68. She did not wash her hands prior to the procedure. She applied gloves, performed the test, removed her gloves and placed the glucometer back into the plastic box on top of the cotton swabs and alcohol pads. She returned to the nurse's station and washed her hands. At 11:52 a.m., LPN AA selected a second resident for point-of-care testing. LPN AA retrieved gloves and the plastic box from the top of the cart. She proceeded to room [ROOM NUMBER]A, R#49. She removed the glucometer from the plastic box and wiped the glucometer with two alcohol pads and performed the test. After performing the test, she replaced the glucometer back into the plastic box, placing the device on top of the cotton swabs and the alcohol pads. An observation of point-of-care testing for blood glucose on 9/6/19 at 12:21 p.m. with LPN BB revealed she placed a clean washcloth on the top of her cart (North-short hall). She retrieved a glucometer device from the drawer of her cart and placed it on the washcloth. She retrieved a plastic box with a flip top from the cart. Inside the box is a glucometer, cotton swabs, alcohol pads and lancets. She removes the glucometer and places it on top of paper towels on the top of the cart. She reported they have two glucometers on their carts. She washed her hands and returned to the cart. She applied gloves and cleaned the glucometer device with a bleach wipe, timing it for five minutes. She removed her gloves, washed her hands, retrieved more gloves and collected the glucometer and the plastic box and went to room [ROOM NUMBER]B, R#13. LPN BB applied gloves, performed the test, placed the glucometer on top of paper towels, removed her gloves, and returned to the cart. She washed her hands; donned gloves and cleaned the glucometer device with bleach wipes for five minutes. An observation of point-of-care testing for blood glucose on 9/6/19 at 12:15 p.m. with LPN CC revealed she placed a clean washcloth on the top of her cart (North-long hall). LPN retrieved two glucometer devices from the drawer of her cart and placed them on her washcloth. She sanitized her hands, placed gloves on her hands and proceeded to clean the glucometers with bleach wipes for five minutes using a timer on top of her cart. LPN CC let the glucometers dry for two minutes. LPN CC sanitized her hands after removing her gloves and gathered one glucometer along with gloves, a plastic box containing cotton balls, alcohol wipes and lancets and went into room [ROOM NUMBER]A, R#42. She applied gloves, performed the test, placed the glucometer on top of paper towels, removed her gloves, returned to the cart to dispose of the lancet in the sharps box, then proceeded to wash her hands. She applied clean gloves and cleaned the glucometer with a bleach wipe for five minutes and placed it back on the clean cloth. At 12:45 p.m. LPN CC selected a second resident for point-of-care testing. She sanitized her hands, gathered the clean, dry glucometer device, gloves and the plastic box, entered room [ROOM NUMBER]-D, R#83. LPN CC applied gloves, performed the test, placed the glucometer on top of paper towels, removed her gloves, returned to the cart disposed of the lancet in the sharps box, washed her hands, applied clean gloves and cleaned the glucometer with a bleach wipe for five minutes, and placed it back on the clean cloth to dry. An interview was conducted with the Director of Nursing (DON) on 9/6/19 at 5:30 p.m. DON revealed the expectations of her nurses regarding cleaning of glucose monitor devices is each nurse on a medication cart should have two glucose monitors. The nurses are to clean the monitors with Clorox wipes for five minutes between each resident, then place the monitors on a clean cloth to let dry, alternating use between the two devices to allow dry time, per our facility policy.
Inspection of April 12, 2019
1 findingBased on record review, review of the facility policy titled Transfer or Discharge/Involuntary of Patients/Residents, facility staff interview, hospital staff interview, Ombudsman interview, and family interview, the facility failed to provide a written 30-day discharge notice that included required information for one resident (R) (#1) out of three residents reviewed for transfer/discharge. Findings include: Review of the policy titled Transfer or Discharge/Involuntary of Patients/Residents dated (MONTH) 2008 revealed the following: The Health Care Center shall give written notice to the Patients/Residents, guardian or representative, if there is no guardian, and the Patients physician at least thirty (30) days before any proposed transfer or discharge is made. The written notice will be on the form provided by the Health Care Center and will contain the following information: the reasons for the proposed transfer or discharge; the effective date of the proposed transfer or discharge, the location or other facility to which the Health Care Center proposed to transfer or discharge the Patient/Resident; and notice of the right to a hearing pursuant to the Georgia Administrative Procedure Act and Section .15 of the Georgia Rules and Regulations Chapter 290-5-39, and of the right to representation by legal counsel. Review of the clinical record for R#1 revealed admission to the facility on [DATE]. Review of the Quarterly Minimum Data Set (MDS) for R#1 dated 1/5/19 revealed the resident had a Brief Interview for Mental Status score of 3 indicating severe cognitive impairment. Review of the Advanced Directives for R#1 revealed if the resident was unable to make health care decisions her (family members) were authorized to make the health care decisions for her. Review of the clinical record for R#1 revealed Social Progress Notes signed by the Administrator with entries as follows: On 2/20/19 .Administrator told (family member) (name) that she would be issuing her a 30-day notice due to the facility not being able to meet her needs. Resident was sent to the hospital on 2/21 (sic) due to her being sick. Calls were made to the hospital for help in placing Resident to another facility. Ombudsman was notified of verbal 30-day on 2/25 (sic). (Name) (Social Service at hospital) called to say Res (sic) wasn't aware of a 30-day notice .Another facility had accepted her. On 2/24/19, family was upset that res (sic) went to another facility. They wanted to appeal the 30-day notice . On 2/25/19, hospital called to talk with Administrator and said hospital had a bed for her at another facility. Admin (sic) told hospital and resident that she would be receiving that 30-day notice that we had talked about. Res (sic) stated she would go ahead and take the other bed. Review of 30-day involuntary discharge notice signed by the Administrator revealed the following: To whom it may concern: On (MONTH) 20, 2019, you (name of R#1) were given a verbal thirty-day notice. On the same day (2/20/19), your (family members) were also notified of the thirty-day notice by phone from the administrator and social service worker. You were sent out to the hospital on (MONTH) 21, 2019. Your thirty-day notice was effective 2/20/19 per the verbal with yourself, your (family members). This is your written thirty-day notice, Thanks (signature of Administrator). Review of hospital discharge planning note dated 2/22/19 signed by the hospital Social Worker (SW) revealed the SW had received a consult for discharge planning. The hospital SW had spoken to a staff person at the nursing home (NH) and was told R#1 had been given a 30-day notice to leave. The NH could not provide the date the notice was given. Continued review of the hospital discharge planning note dated 2/25/19 revealed that the hospital SW had met with R#1 and she wanted to return to the NH and denied receiving a notice from the NH regarding leaving in 30 days. The hospital SW spoke with the NH Administrator and she revealed she had given R#1's (family member) a verbal notice and stated that they could not accept R#1 back. The SW explained to R#1 that she had two choices, to go to another facility that had accepted her or have her family take her home. R#1 told the SW that she would go to the other facility. An interview with the Ombudsman on 3/25/19 at 4:52 p.m. revealed she had requested a written 30-day discharge notice on 2/25/19 and received the notice on 2/26/19 at 4:24 p.m. The Ombudsman revealed she had noted that the notice was not dated and did not include information related to the specific needs that the facility could not meet or the right to appeal the discharge notice and the right to legal counsel. The Ombudsman revealed when she had asked the facility SW for a copy of the written discharge notice, the SW was not aware the facility was required to send the Ombudsman a copy of the notice prior to the discharge. During an interview on 3/26/19 at 10:03 a.m., Family A of R#1 revealed he had been told several times by the Administrator and the SW at the facility over the past year that the family had 30 days to find R#1 another facility to go to. However, he had never, including the last time on 2/20/19, been informed of this in writing or of the right to an appeal, what specific needs the facility could not meet, or of the right to legal counsel. Family A of R#1 revealed he had been surprised when he received a call from a staff person at the nursing home informing him that R#1 was not coming back and was going to another nursing home. Family A revealed R#1 is happy at the new nursing home and he is now satisfied that the resident was transferred somewhere else, but the family would have appealed the discharge if they had been given the chance. During an interview on 3/26/19 at 10:19 a.m., Family B of R#1 revealed she had never received a written 30-day discharge notice and was aware the notice had to be in writing to be valid. Family B revealed she had not been informed in writing or verbally of the right to appeal the discharge or the right to legal counsel; and she would have immediately appealed the notice if she had received anything in writing. Family B revealed she had been told by the Administrator verbally that the family would have to find another nursing home for R#1 on 2/20/19 and had been told this at other times as well, but R#1 had always been accepted back from the hospital and the family never received anything in writing. During an interview on 3/26/19 at 4:30 p.m., the Administrator revealed she had never given a 30- day notice in writing to R#1 or her family and had given a verbal notice to the family and R#1 on 2/20/19. The Administrator revealed she had requested the assistance of the hospital to place R#1 in another facility. The Administrator acknowledged she was aware that the family of R#1 would have appealed the discharge. The Administrator revealed she had never told anyone at the hospital that R#1 could not return to the facility; but had said that if she returned, she would be given the 30-day notice effective on the date of the verbal notice. An interview with the facility Medical Director on 4/8/19 at 10:02 a.m. revealed he and the Administrator, Director of Nursing (DON) and SW had discussed finding another nursing home for R#1 and giving a 30 day-notice, but he was unaware of any concrete plans. An interview with the hospital SW on 4/12/19 at 9:00 a.m. revealed she had been informed by the facility SW and the facility Administrator that R#1 could not be transferred back to the facility. The SW revealed that on 2/22/19, she had been informed by the Administrator that R#1 and her family had been given a 30-day notice and her assistance had been requested to find R#1 another facility for transfer after hospital discharge. The hospital SW revealed she had asked the facility SW when the 30-day notice had been given to R#1 and her family and never received an answer. The hospital SW revealed she had again discussed the discharge of R#1 with the Administrator while in the room of R#1 on 2/25/19. R#1 had told her she never received a 30-day notice. The hospital SW had informed R#1 while on the phone with the Administrator that R#1 could not return to the facility and would have to be transferred to another nursing home or go home with her family. Further interview with the facility Administrator on 4/12/19 at 10:17 a.m. revealed she did not think a written 30-day notice was necessary because R#1 had agreed to go to another facility.
Inspection of June 14, 2018
2 findingsBased on interview, review record and review of facility policy, it was determined the facility failed to notify the responsible party of a change in medication for one resident from a sampled 29 residents. (Resident {R} #12) Findings include: Telephone interview conducted with the R #12's family member (responsible party) on 6/11/18 at 6:38 p.m. revealed the family stated the resident had just returned from the hospital after having a [MEDICAL CONDITION] (GI Bleed). The family member also stated the bleeding was due to the resident not receiving her medication ([MEDICATION NAME]) for gastro-[MEDICAL CONDITION] reflux disorder (GERD). The family member further stated he could not understand why the facility never called to inform him that the resident was no longer taking the medication. Her family member further stated he feels stopping the medication contributed to this episode of bleeding. The family member was also concerned the facility never informed him that R #12 had returned to the facility. But most importantly he would like an explanation as to why the medication was discontinued. Review of the resident's most recent quarterly Minimum Data Set ((MDS) dated [DATE] revealed the resident was assessed severe cognition impairment and required total assistance will with activities of daily living (ADLs). A review of the facility document titled Facility [DIAGNOSES REDACTED]. Review of (MONTH) to (MONTH) physician's monthly orders show the resident on Pantoprazole ([MEDICATION NAME]) 40 milligrams (mg) one tab daily for GERD. Review of Pharmacy Consultant notes dated 5/18/18 revealed the pharmacist made a recommendation to Please add Not Crush Medications to the following medications orders. Review of physician's (MD) telephone order dated 5/29/18 documents to Discontinue (D/C) [MEDICATION NAME]. A review of the nurse's notes failed to reveal R #12 's family member was notified of the decision to discontinue the resident's medication. Review of the MD's progress notes failed to reveal documentation as to why medication was discontinued. Further review of the nurses' notes and the physician's progress notes failed to reveal documentation of notification of the resident's family member that the resident's medication was discontinued. A review of the resident's Medication Administration Record [REDACTED]. Review of the nurses' notes dated 6/7/18 documents resident having coffee ground emesis all week long. Resident has been off [MEDICATION NAME] for a week via pharmacy reconciliation. Further record review reveals R #12 sent to the emergency room (ER) on 6/7/18 and was admitted to the hospital on [DATE] with [DIAGNOSES REDACTED]. Review of the emergency room 's history and physical for the resident (HP) dated 6/9/18 documents resident has not been given the [MEDICATION NAME] and it was unknown how long the resident had not received the medication. Also, the resident had progressive [MEDICAL CONDITION] was without medication. An interview with Licensed Practical Nurse (LPN) AA on 6/13/18 at 11:30 a.m. outside the resident's room revealed the resident had been taking the [MEDICATION NAME] for a couple of years and the Pharmacy Consultant decided to discontinue the medication. LPN AA also stated the medication was probably discontinued as a cost control measure for the pharmacy. The LPN stated the pharmacy did notify the facility. LPN AA was asked if the resident's primary care physician (PCP) was notified. LPN AA stated she was not sure if the physician was notified. LPN AA also stated sometimes they could give a substitute medication but felt it would not be as effective as [MEDICATION NAME]. The LPN thinks the resident went without the medication for two weeks. LPN AA noticed the resident had a couple of episodes of coffee grounds emesis and notified supervisor for confirmation and then notified MD to send resident out for evaluation. However, the LPN did not notify the resident's family member. An interview was conducted on 6/14/18 at 8:30 a.m. with the Assistant Director of Nursing (ADON) and the Director of Nursing (DON) in their office. It was revealed when the Pharmacy Consultant completes the Drug Regimen Review (DRR) he gives the documents to the ADON and DON, they in turn review the documents with the facility physician and have him sign off, then make the recommendations on the resident charts and keep a copy in their office. The administrative nurses stated there was a problem with the resident taking her medications and the nurses had been crushing her medications. The Pharmacist had recommended not to crush this medication. When the administrative nurses made the physician aware of the recommendation the physician decided to discontinue the medication. Both administrative nurses agreed the resident's family should have been notified of the discontinuation of the resident's medication but was not. The DON stated that it is not policy for the facility to notify a family member when a resident return to the facility from the hospital, that is the responsibility of the hospital. A telephone interview with the Medical Director was conducted on the 6/14/18 at 12:30 p.m. The Medical Director stated although he was not the resident's primary care physician he agreed with the decision to discontinue the resident's [MEDICATION NAME]. The resident was having trouble swallowing her medications and a decision was made to crush her pills. After the Pharmacist's recommendation the Physician had to make a decision which would be best for the resident either give the resident the medication and take a chance on her choking or discontinue the medication and see if she experiences any problems. Unfortunately, the resident did have a GI bleed and is back on the medication. The Medical Director further stated since the resident's swallowing ability decreases they will need to look at another medication to help with the resident's GI problems. A review of a facility document titled Notifying Physicians and Family of Resident's Condition (undated) failed to revealed notification of family when there is a change in the resident's treatment or medication.
Based on observation, interview, and record review, it was determined the facility failed to ensure one resident from a sampled 29 residents received the appropriate care and services for a Foley catheter. (Resident {R} #88). Findings include: An observation on 6/12/18 at 2:15 p.m. revealed R #88 in his bed positioned on his back waiting to receive wound care. The resident's Foley drainage bag laying on top the foot of resident's bed. The resident's catheter was had yellow urine with slight amount sediment in the tubing draining back into the resident. The resident was overheard complaining about in his lower abdomen and burning on urination. Nurse CC was overheard telling the resident as soon as the wound care was completed she would bring him something for pain. The resident received wound care the pressure areas on his hip and sacral areas. During the entire time the wound care was provided (approximately 20 minutes) the resident's urinary drainage bag remained in the bed at bladder level. After wound care was completed Nurse CC inquired about the resident's pain level and location. The resident responded by pointing to his lower abdominal area and that pain score was around eight or nine. Neither Nurse or the WCN (Wound Care Nurse) had noticed the resident's urinary drainage bag was in the bed with the resident and urine was backing up into the resident. The surveyor asked if the resident's drainage bag was in the correct position. Both nurses agreed the drainage bag should be positioned on the side of the bed below the resident's bladder. Nurse CC and WCN reposition the resident and positioned drainage bag below the resident's bladder. The resident stated he was starting to feel better and would not require pain medication. Both nurses proceeded to the resident's catheter tubing strap and identified the catheter tubing was kinked. Once the catheter was unkinked R #88 stated that he felt much better. Nurse CC stated it look like the clamp on the strap was not closed correctly on the catheter. Both nurses agreed the improper position of the drainage bag and the catheter strap could have possibly contributed to the resident's complaint of discomfort and the urinary burning. Record review reviewed revealed R #88 was admitted to the facility with [DIAGNOSES REDACTED]. A review of the (MONTH) physician's orders [REDACTED]. An interview was conducted on 6/12/18 at 2:40 p.m. with Certified Nursing Assistant (CNA) DD outside R#88's room revealed the she was assigned to the resident that day. CNA DD stated that she had assisted the resident to bed so that he could have his dressing changed. CNA DD also stated that a resident with Foley catheter should have the drainage bag positioned below the resident's bladder area. The CNA that she forgot the drainage bag was left in the bed with the resident as she was called away to assist with another resident and thought the nurse would position the drainage bag since the nurses was preparing to provide wound care to the resident.
Inspection of July 20, 2017
1 findingBased on observation, interview, and record review, the facility failed to ensure food was prepared, stored, and served in a sanitary manner. This had the potential to affect 87 of 87 residents receiving food from the facility kitchen. Findings include: 1. On 7/17/17 the following observations were made in the facility kitchen: a. At 9:30 a.m. the 22 Multi-Quat Sanitizer in the third compartment of the three-compartment sink was measured using test strips by the Dietary Supervisor (DS). The level of the sanitizer was 100 parts per million (ppm). Review of the manufacture instructions for the 22 Multi-Quat Sanitizer provided by the DS and as posted on the wall above the three-compartment sink revealed the sanitizer level of the sanitizer was supposed to be between 150 and 400 ppm to sanitized cook ware and food contact surfaces. The DS verified the sanitizer was at 100 ppm. During the tour of the kitchen, on 7/17/17 at 9:30 a.m., the shelf over the stove was soiled with dried food substances and a greasy build up; the two gas ovens and the top of the gas six burner stove was soiled with a heavy buildup of food and black substance; the wall behind the oven and behind the three-compartment sink were soiled with a dried substance. At 9:30 a.m. the outside surface of the four 96-gallon containers containing flour, sugar, thickener, and corn meal were each soiled with a build-up of dried sticky food residue on the lids and the sides of the large container. Inside the container of the white thickener was a black round item about 1/8th of an inch long. The DS verified all four containers were each soiled and upon request removed the black 1/8 substance out of the thickener using a measuring cup. He stated he did not know what the substance was but verified it was not part of the thickener. Also observed, during this time, was a fan mounted on the wall that was blowing into the kitchen food preparation area. It had a heavy buildup of dirt and dust. The DS acknowledged that the fan was dirty. b. At 7/17/17 at 9:33 a.m. two containers of sanitizing solution containing the wiping clothes were tested by the DS using test strips. When the DS compared the strip to the color coding on the outside of the test strip container the 22 Multi-Quat Sanitizer solution was less than 50 ppm. The DS verified the solution was not strong enough to sanitize the food preparation surfaces. Both of the containers were located in the food preparation areas. At 9:35 a.m. Cook BB was interviewed about the sanitizing solution. She verified she used the solution to clean the food preparation surfaces and stated she made the solution up at 6:00 a.m. that morning. Review of the manufacture instructions for the 22 Multi-Quat Sanitizer provided by the DS and as posted on the wall above the three-compartment sink revealed the sanitizer level of the sanitizer was supposed to be between 150 and 400 ppm to sanitized cook ware and food contact surfaces. The DS verified the sanitizer was at 100 ppm. c. At 9:40 a.m. one closed food cart and two open food carts were set up with clean trays for the next meal. The DS verified the carts were being set up for the next meal. Inspection of the carts revealed each of the carts were soiled with sticky and dried food residue. He verified the carts had not been cleaned and sanitized prior to being set up with clean trays for the next meal. It was also noted at this time, the filters in the hood over the oven were soiled with a heavy black build up. The DS verified there was a heavy black build up. On 7/17/17 at 9:40 a.m. condensation was dripping from two air intake vents located on the ceiling of the kitchen. One of the vents was located over the food service preparation counter and the second vent was located over the open cart which had been set up with trays for the lunch meal. On 7/19/17 at 11:29 a.m. a full sheet pan containing 24 glasses of tea was sitting on the counter under the vent. The condensation was actively dripping from the vent and onto the uncovered glasses of tea. The DS verified the condensation from the vent on the ceiling was dripping into the glasses of beverages. After being informed of the condensation dripping into the beverages and verifying the observation he moved the beverages to a cart. At 12:00 p.m. the food service worker moved the beverages back to the counter and served the same beverages. During the 7/17/17 9:40 a.m. kitchen observations, the Food Service Employee (FSE) EE was observed to rack up the dirty silverware and use his bare hands to spread the silverware out in the rack prior to running it through the dish washer. After pushing the dirty silverware through into the dish washer he went to the clean end of the dish washer and started wiping his hands on a dish towel located on the surface of the clean end of the dish washer. The DS verbally prompted FSE EE to sanitize his hands. After being verbally prompted FSE EE went back to the dirty end of the dish washer and applied hand sanitizer on his hands from a dispenser located of the dirty end of the dish washer. After applying the sanitizer to his hands, he quickly rubbed his hands together and returned to the clean end of the dish washer and unloaded the plates from a rack located at the clean end of the dish washer. The policy for dish washing and hand washing and the manufacture instructions for the use of the hand sanitizer was requested. Review of the undated Hand Washing policy revealed alcohol based hand rub should only be used if hands are not visibly soiled. According to an email from the sanitizer supply company (the facility could not provide the manufacture instructions) provided by the facility in lieu of the manufacture guidelines documented staff were to make sure all organic matter like dirt and grease were removed from hands, to apply a dime-size amount to the palm of the hands and to rub hands together covering all surfaces for 30 seconds to allow hands to completely absorb the product and the hand sanitizer to dry. On 7/19/17 at 11:30 a.m. the DS verified the employee did not rub his hands together for 30 seconds. He stated the employee should have been wearing gloves when racking dirty dishes and then removed the gloves prior to applying the sanitizer. d. At 9:45 a.m. there was a bag of egg patties, potato tots, and a bag of biscuits in the reach in freezer without a label or dates. The freezer contained an open box of biscuits that were not proper sealed as the bag in the box was not sealed closed. The deep fat fryer was soiled with a heavy buildup of food crumbs and the baskets for the deep fat fryer were sitting on a sheet pan that was also soiled with grease and food crumbs. The DS verified these observation. 2. On 7/19/17 at 11:15 a.m. two food carts with doors and two open carts were inspected with the assistance of the DS. The carts were set up with trays for the noon meal. The carts with the doors were noted to have a dried sticky substance on the underside of the metal brackets that hold the food trays. The open carts were also noted to have a dried brown food residue on the outer portion of the metal carts. The DS verified the carts had not been thoroughly cleaned and sanitized prior to being set up for the noon meal service. He stated the carts are used to deliver the food trays to the resident and then the dirty trays were loaded in the carts and returned to the kitchen. 3. Observations of the kitchen, on 7/19/17 at 11:15 a.m., revealed the shelf over the oven, the ovens and stove top, and the shelf under the food service counter, containing the containers of salt and pepper and sweeteners, remained soiled with a dried residue. 4. On 7/20/17 at 10:50 a.m. the containers of sanitizing solution, in the kitchen, were checked by the DS. The container of sanitizing solution located by the stove was 50 ppm. The DS verified the solution was not strong enough to sanitize the food contact/preparation surfaces.
← Back to the Evergreen Health and Rehabilitation Center record
Deficiency Index is independent and is not affiliated with, endorsed by, or approved by CMS, Medicare, or any government agency. About this data · Report a correction