F 0641
Ensure each resident receives an accurate assessment.
Level of Harm - Minimal harm
or potential for actual harm
**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** 3. Review of
Resident #90's medical record revealed an admission date of [DATE] with admission diagnoses of bladder
cancer, myocardial infarction and congestive heart failure. Resident #90 was discharged to home on
[DATE].
Residents Affected - Some
Further review of the medical record found no evidence of hospital readmission during admission to the
facility.
Review of the MDS 3.0 discharge assessment completed on [DATE] indicated Resident #90 was
discharged to an acute hospital.
On [DATE] at 3:55 P.M. interview with RN #300 verified the MDS 3.0 assessment for Resident #90 was
incorrectly coded as the resident being discharged to an acute hospital when the discharge location was
home.
4. Review of Resident #1's medical record revealed an admission date of [DATE]. Further review of the
medical record revealed Resident #1 expired in the facility on [DATE]. Review of Resident #1's MDS 3.0
assessments revealed the last assessment completed was a quarterly MDS 3.0 comprehensive
assessment with a reference date of [DATE]. There was no evidence an MDS assessment was completed
to identify Resident #1 expired in the facility.
On [DATE] at 11:50 A.M. interview with RN #300, verified no MDS 3.0 assessment was completed after
Resident #1 expired.
Based on medical record review and interview the facility failed to ensure Minimum Data Set (MDS) 3.0
assessments were accurately completed. This affected four residents (#1, #38, #56 and #90) of 28
residents whose MDS 3.0 assessments were reviewed.
Findings include:
1. Review of Resident #38's medical record revealed diagnoses including cerebral palsy, type 2 diabetes,
moderate intellectual disabilities, and chronic obstructive pulmonary disease.
On [DATE], a physician's order was written to admit Resident #38 to Hospice with end stage senile
degeneration of the brain. A significant change in status Minimum Data Set (MDS) 3.0 assessment dated
[DATE] did not reveal Resident #38 was receiving hospice.
On [DATE] at 9:46 A.M., Registered Nurse (RN) #300 verified the significant change MDS 3.0 assessment,
dated [DATE] was coded incorrectly and should have indicated Resident #38 was receiving Hospice
(continued on next page)
Any deficiency statement ending with an asterisk (*) denotes a deficiency which the institution may be excused from correcting providing it is determined that other
safeguards provide sufficient protection to the patients. (See instructions.) Except for nursing homes, the findings stated above are disclosable 90 days following the
date of survey whether or not a plan of correction is provided. For nursing homes, the above findings and plans of correction are disclosable 14 days following the date
these documents are made available to the facility. If deficiencies are cited, an approved plan of correction is requisite to continued program participation.
LABORATORY DIRECTOR'S OR PROVIDER/SUPPLIER
REPRESENTATIVE'S SIGNATURE
TITLE
(X6) DATE
FORM CMS-2567 (02/99)
Previous Versions Obsolete
Facility ID:
If continuation sheet
Page 1 of 5
Event ID:
365402
Printed: 05/15/2026
Form Approved OMB
No. 0938-0391
Department of Health & Human Services
Centers for Medicare & Medicaid Services
STATEMENT OF DEFICIENCIES
AND PLAN OF CORRECTION
(X1) PROVIDER/SUPPLIER/CLIA
IDENTIFICATION NUMBER:
(X2) MULTIPLE CONSTRUCTION
365402
B. Wing
A. Building
(X3) DATE SURVEY
COMPLETED
10/24/2019
NAME OF PROVIDER OR SUPPLIER
STREET ADDRESS, CITY, STATE, ZIP CODE
Altercare of Alliance Ctr for Rehab & NC Inc
11750 Klinger Avenue NE
Alliance, OH 44601
For information on the nursing home's plan to correct this deficiency, please contact the nursing home or the state survey agency.
(X4) ID PREFIX TAG
SUMMARY STATEMENT OF DEFICIENCIES
(Each deficiency must be preceded by full regulatory or LSC identifying information)
F 0641
services and had a life expectancy less than six months.
Level of Harm - Minimal harm
or potential for actual harm
2. Review of Resident #56's medical record revealed diagnoses including generalized muscle weakness,
difficulty walking, legal blindness, and chronic obstructive pulmonary disease.
Residents Affected - Some
A nursing note dated [DATE] at 6:03 A.M. indicated Resident #56 was observed on the floor in her room. An
incident reassessment summary dated [DATE] indicated Resident #56 stated she going to the bathroom
and slipped and fell.
An annual MDS 3.0 assessment, dated [DATE] indicated Resident #56 was cognitively intact and required
supervision for walking in her room and in the corridor. The MDS indicated Resident #56 had no falls since
the prior assessment completed on [DATE].
On [DATE] at 2:05 P.M., RN #300 verified the [DATE] MDS 3.0 assessment for falls was coded incorrectly
as Resident #56 did have a fall.
FORM CMS-2567 (02/99)
Previous Versions Obsolete
Event ID:
Facility ID:
365402
If continuation sheet
Page 2 of 5
Printed: 05/15/2026
Form Approved OMB
No. 0938-0391
Department of Health & Human Services
Centers for Medicare & Medicaid Services
STATEMENT OF DEFICIENCIES
AND PLAN OF CORRECTION
(X1) PROVIDER/SUPPLIER/CLIA
IDENTIFICATION NUMBER:
(X2) MULTIPLE CONSTRUCTION
365402
B. Wing
A. Building
(X3) DATE SURVEY
COMPLETED
10/24/2019
NAME OF PROVIDER OR SUPPLIER
STREET ADDRESS, CITY, STATE, ZIP CODE
Altercare of Alliance Ctr for Rehab & NC Inc
11750 Klinger Avenue NE
Alliance, OH 44601
For information on the nursing home's plan to correct this deficiency, please contact the nursing home or the state survey agency.
(X4) ID PREFIX TAG
SUMMARY STATEMENT OF DEFICIENCIES
(Each deficiency must be preceded by full regulatory or LSC identifying information)
F 0689
Level of Harm - Minimal harm
or potential for actual harm
Residents Affected - Few
Ensure that a nursing home area is free from accident hazards and provides adequate supervision to
prevent accidents.
**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** Based on
observation, medical record review, review of Material Safety Data sheets (MSDS) and interview the facility
failed to supervise the whereabouts of a resident on the dementia unit resulting in Resident #29 being
located in a storage room unsupervised. This affected one resident (#29) of 22 residents residing on the
unit.
Findings include:
Review of Resident #29's medical record revealed an admission date of 08/01/17. Diagnoses included
cognitive communication deficit, history of suicidal ideation, difficulty walking, depression, dementia, history
of falling, and cerebrovascular disease. Resident #29 resided in a secured dementia unit.
A quarterly Minimum Data Set (MDS)3.0 assessment dated [DATE] indicated Resident #29 was sometimes
able to make himself understood and was sometimes able to understand others. Resident #29 was
assessed with impaired vision (able to see large print). An assessment of his mental status revealed
Resident #29 was severely cognitively impaired. The MDS indicated Resident #29 wandered 4-6 days of
the assessment reference period. Resident #29 was assessed as requiring extensive assistance with
transfers and locomotion on the unit. Resident #29 did not walk. Resident #29 used a wheelchair for
mobility. Review of Resident #29's care plan revealed behaviors included wandering at times, jiggling
random door handles, wandering in and out of other resident rooms, and using. other residents' restrooms.
On 10/22/19 at 11:45 A.M., while a Safety and Health Consultant was touring the facility, Resident #29 was
observed in a storage room (which locked from the corridor side) unattended on the secure dementia unit.
The door had a key code which Maintenance Staff #302 had to enter to unlocked the door from the outside.
The door also had a self-closing device. Resident #29 was sitting in his wheelchair with his leg positioned in
front of the door making it difficult to open. The room contained shelves with multiple wash basins with
personal care products in them including mouth wash, toothpaste, and body wash. Behind Resident #29's
wheelchair was an unlocked cabinet with items including hand sanitizer, perineal cleaner, moisturizing
cream, mouth wash, toothpaste, shave cream and body wash. Maintenance Staff #302 tested the door
function three times after Resident #29 was removed from the room with no problems noted with its
functioning.
On 10/24/19 at 1:35 P.M., Maintenance Staff #302 stated he had worked at facility since April 2019 and had
never been told there was a problem with the lock or closure of the storage room on the secure unit where
Resident #29 was located unsupervised.
Review of MSDS sheets for the products in the storage room were reviewed. The MSDS for Dawnmist
[NAME] Gel fluoride toothpaste revealed if the product was ingested the material was to be removed from
the mouth and the mouth rinsed. Call a physician or Poison Control Center immediately. The MSDS for
DawnMist mouth rinse indicated if the product came into contact with eyes the eyes were to be rinsed
immediately with plenty of water for at least 15 minutes. If the product was ingested, a physician or Poison
Control Center were to be contacted. The MSDS for Dawnmist Brushless Shave Cream indicated if the
product was ingested a physician or the Poison Control Center should be contacted immediately. The
MSDS for Secura Personal Cleanser indicated if the product was ingested, the Poison Control
(continued on next page)
FORM CMS-2567 (02/99)
Previous Versions Obsolete
Event ID:
Facility ID:
365402
If continuation sheet
Page 3 of 5
Printed: 05/15/2026
Form Approved OMB
No. 0938-0391
Department of Health & Human Services
Centers for Medicare & Medicaid Services
STATEMENT OF DEFICIENCIES
AND PLAN OF CORRECTION
(X1) PROVIDER/SUPPLIER/CLIA
IDENTIFICATION NUMBER:
(X2) MULTIPLE CONSTRUCTION
365402
B. Wing
A. Building
(X3) DATE SURVEY
COMPLETED
10/24/2019
NAME OF PROVIDER OR SUPPLIER
STREET ADDRESS, CITY, STATE, ZIP CODE
Altercare of Alliance Ctr for Rehab & NC Inc
11750 Klinger Avenue NE
Alliance, OH 44601
For information on the nursing home's plan to correct this deficiency, please contact the nursing home or the state survey agency.
(X4) ID PREFIX TAG
SUMMARY STATEMENT OF DEFICIENCIES
(Each deficiency must be preceded by full regulatory or LSC identifying information)
F 0689
Level of Harm - Minimal harm
or potential for actual harm
Center or physician should be contacted immediately for instructions. The MSDS for the Secura Personal
Cleanser revealed the product was harmful if swallowed, caused skin irritation, could cause an allergic skin
reaction, and caused serious eye damage and eye irritation. The MSDS for Secura Protective Cream
revealed if ingested, a Poison Control Center or physician should be contacted immediately if ingested.
Residents Affected - Few
FORM CMS-2567 (02/99)
Previous Versions Obsolete
Event ID:
Facility ID:
365402
If continuation sheet
Page 4 of 5
Printed: 05/15/2026
Form Approved OMB
No. 0938-0391
Department of Health & Human Services
Centers for Medicare & Medicaid Services
STATEMENT OF DEFICIENCIES
AND PLAN OF CORRECTION
(X1) PROVIDER/SUPPLIER/CLIA
IDENTIFICATION NUMBER:
(X2) MULTIPLE CONSTRUCTION
365402
B. Wing
A. Building
(X3) DATE SURVEY
COMPLETED
10/24/2019
NAME OF PROVIDER OR SUPPLIER
STREET ADDRESS, CITY, STATE, ZIP CODE
Altercare of Alliance Ctr for Rehab & NC Inc
11750 Klinger Avenue NE
Alliance, OH 44601
For information on the nursing home's plan to correct this deficiency, please contact the nursing home or the state survey agency.
(X4) ID PREFIX TAG
SUMMARY STATEMENT OF DEFICIENCIES
(Each deficiency must be preceded by full regulatory or LSC identifying information)
F 0880
Provide and implement an infection prevention and control program.
Level of Harm - Minimal harm
or potential for actual harm
Based on observation, policy review, manufacturer guidelines review and interview the facility failed to
maintain adequate infection control practices related to the use of a shared glucometer to prevent the
spread of infection. This had the potential to affect four residents (#34, #57, #58 and #89) of four residents
identified to be diabetic and who could use glucometer testing on the 211-222 rooms medication cart.
Residents Affected - Few
Findings include:
On 10/22/19 at 11:30 A.M. Licensed Practical Nurse (LPN) #301 was observed using a glucometer to
obtain Resident #34's blood glucose level. The blood glucose level was obtained and LPN #301 returned to
the medication cart in the hallway. At 11:33 A.M., LPN #301 used one Clorox wipe to clean the glucometer.
LPN #301 wiped the glucometer for approximately three seconds and placed the glucometer back into the
top drawer of the medication cart, failing to ensure the glucometer maintained an appropriate contact time
with the Clorox wipe.
At 11:37 A.M., review of the Clorox wipes with LPN #301 indicated proper disinfection of surfaces required
a contact time of three minutes for Clostridium difficile (C-Diff), 30 seconds for bacteria, one minute for
viruses and one minute for blood borne pathogens.
On 10/22/19 at 11:38 A.M., interview with LPN #301 verified the glucometer was wiped for three seconds
and did not maintain contact time with the Clorox wipe as per the manufacturer's recommendations.
Review of the undated facility policy and procedure titled Fingerstick Glucose Level revealed to follow
bleach germicidal wipe contact time list.
Review of the Clorox Healthcare Bleach Germicidal Wipes Manufacturer's Instructions revealed: To
disinfect, all surfaces were to remain wet for contact time listed: bacteria 30 seconds, viruses 1 minute,
C-Diff 3 minutes.
FORM CMS-2567 (02/99)
Previous Versions Obsolete
Event ID:
Facility ID:
365402
If continuation sheet
Page 5 of 5