F 0638
Assure that each resident’s assessment is updated at least once every 3 months.
Level of Harm - Minimal harm
or potential for actual harm
Based on interview and record review, the facility failed to timely transmit Minimum Data Set (MDS)
Assessments for 2 (R20 & R25) of 2 residents reviewed for timely MDS submission in the sample of 45.
Residents Affected - Few
The findings include:
1. R20's Face Sheet documented an admission date of 11/20/2024 and included diagnoses of Chronic
Obstructive Pulmonary Disease, Anxiety, and Depression. This same document listed a discharge date of
12/5/24.
R20's last transmitted MDS was an admission assessment and was completed on 11/27/24.
2. R25's Face Sheet documented an admission date of 10/29/2024 and included diagnoses of repeated
falls, anemia, type 2 diabetes, and muscle weakness. This same document listed a discharge date of
11/26/24.
R20's last transmitted MDS was an admission assessment and was completed on 11/5/24.
On 4/23/25 at 11:00 AM, V4 (MDS Coordinator) stated that she just took over this job in March of 2025 and
recognizes that R20 and R25's assessments are showing up as overdue quarterly assessments, however a
discharge assessment should have been completed and transmitted with a due date of 12/5/24 for R20,
and a discharge assessment should have been completed and transmitted with a due date of 11/26/25 for
R25.
On 4/24/25 at 11:30 AM, V4 stated that she had completed and transmitted the discharge MDS's for R20
and R25.
Review of the final validation report documents that R20's discharge assessment target date was
12/05/2024, but was not transmitted as complete until 4/24/25 and documents a message that the
completion date is more than 14 days after the assessment reference target date. This same report
documents that R25's discharge assessment target date was 11/26/24, but was not transmitted as
complete until 4/24/25 and documents the same message that the completion date is more than 14 days
after the assessment reference target date.
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 3
Event ID:
146019
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
146019
B. Wing
A. Building
(X3) DATE SURVEY
COMPLETED
04/25/2025
NAME OF PROVIDER OR SUPPLIER
STREET ADDRESS, CITY, STATE, ZIP CODE
Wabash Senior Living & Rehab
216 College Boulevard
Carmi, IL 62821
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 0760
Ensure that residents are free from significant medication errors.
Level of Harm - Minimal harm
or potential for actual harm
**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** Based on
interview and record review, the facility failed to ensure residents received the correct medications in
accordance with their physician's orders for 2 (R83, R92) of 7 residents reviewed for significant medication
errors in the sample of 45.
Residents Affected - Few
This past noncompliance occurred between 3/17/2024 and 4/1/2025.
Findings include:
1. R83's admission Record documented an admission date of 3/13/2024 and included diagnoses of
unspecified dementia, unspecified severity, without behavioral disturbance, psychotic disturbance mood,
anxiety disorder, unspecified, and unspecified atrial fibrillation.
R83's Minimum Data Set (MDS) dated [DATE] documented a Brief Interview for Mental Status (BIMS) score
of 5, which indicates severe cognitive impairment.
R83's Physician Order Summary documented divalproex (seizure and/or mood stabilization treatment) oral
tablet delayed release 500mg (milligrams) -1 tablet by mouth twice a day, acetaminophen (pain reliever)
oral tablet 500mg-give 2 tablets by mouth two times a day and apixaban (blood thinner) 5mg tablet-take 1
tablet by mouth twice a day.
R83's Progress Note dated 3/17/2025 by V3 (Registered Nurse/RN) documented that she was passing
medications and took R83 and R92 back to their shared room. V3 documented that she heard a conflict up
the hall that made her accidentally mix up the unlabeled medication cups. V3 documented R83 was given
R92's medications including donepezil (dementia treatment) 5mg.
2. R92's admission Record documented an admission date of 8/8/2024 and included diagnoses of
unspecified dementia, unspecified severity, without behavioral disturbance, psychotic disturbance mood,
altered mental status and muscle weakness.
R92's MDS dated [DATE] documented a BIMS score of 3, which indicates severe cognitive impairment.
R92's Physician Order Summary documented donepezil hydrochloride (dementia treatment) 5mg-1 tablet
by mouth at bedtime and memantine (dementia treatment) 10mg tablet, take 1 tablet by mouth twice a day.
R92's Progress Note dated 3/17/2025 by V3 (RN) documented that she was passing medications and took
R92 and R83 back to their shared room. V3 documented that she heard a conflict up the hall and
accidentally swapped the medication cups. V3 documented R92 was given R83's medications including
acetaminophen 1000mg, valproate 500mg and apixaban 5mg.
On 04/24/25 at 10:00 AM, V1 (Administrator) stated, he had been notified by V3 (RN) that she administered
the wrong medications to R83 and R92. V1 stated, he advised V3 to contact V2 (Director of Nursing/DON)
and then he immediately started working on the plan of correction that included education and observation
of medication administration by nursing staff.
On 04/24/25 at 10:36 AM, V2 (DON) stated, she was notified via phone by V3 (RN) that she had given
(continued on next page)
FORM CMS-2567 (02/99)
Previous Versions Obsolete
Event ID:
Facility ID:
146019
If continuation sheet
Page 2 of 3
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
146019
B. Wing
A. Building
(X3) DATE SURVEY
COMPLETED
04/25/2025
NAME OF PROVIDER OR SUPPLIER
STREET ADDRESS, CITY, STATE, ZIP CODE
Wabash Senior Living & Rehab
216 College Boulevard
Carmi, IL 62821
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 0760
Level of Harm - Minimal harm
or potential for actual harm
Residents Affected - Few
R83 and R92 the wrong medications. V2 stated V5 (Physician) was contacted, vitals were obtained on R83
and R92 with monitoring scheduled for every 2 hours for the next 24 hours. V2 stated V1 immediately
started a plan of correction that included education and auditing of the nursing staff being observed during
medication administration on 10 residents.
The facility policy Adverse Consequences and Medications Error (revised April 2014) documented under
Policy The interdisciplinary team evaluates medication usage in order to prevent and detect adverse
consequences and mediation-related problems such as adverse drug reactions (ADRs) and side effects.
Adverse consequences shall be reported to the Attending Physician and Pharmacist, and to federal
agencies as appropriate. Under Policy, 5. A medication error is defined as the preparation or administration
of drugs or biological which is not in accordance with physician's orders, manufacturer specifications, or
accepted professionals' standards and principles of the professional(s) providing services.
Prior to the survey date, the facility took the following actions to correct the non-compliance:
1. Incident Investigation of 2 residents on one wing had received the wrong medication during the bedtime
medication pass.
2. Per review of the Interdisciplinary team, it is felt that there is potential for other residents.
3. Staff member had been offered education regarding 5 rights of medication administration. Completed by
4/1/2025. Mediation Administration rate at 0% during survey.
4. All nursing staff to be educated regarding 5 rights of medication administration. Completed by 4/1/2025,
Medication Administration rate at 0% during survey.
5. The Administrator/Director of Nursing and/or designee will observe return demonstration of medication
on each nurse with 10 residents med passes being observed. V2 completed audits by 4/1/2025 with V1 and
V2 in attendance.
6. QAPI (Quality Assurance Performance Improvement) meeting held - any issue identified will be
immediately corrected and re-education will be offered and reviewed during QAPI meeting. This was also
completed by 4/1/25.
FORM CMS-2567 (02/99)
Previous Versions Obsolete
Event ID:
Facility ID:
146019
If continuation sheet
Page 3 of 3