F 0755
Level of Harm - Minimal harm
or potential for actual harm
Residents Affected - Few
Provide pharmaceutical services to meet the needs of each resident and employ or obtain the services of a
licensed pharmacist.
Based on review of medical record, staff interview, and review of facility policy, the facility failed to ensure
physician ordered medications were available for administration. This affected two residents (#26 and #80)
of five (#26, #71, #80, #89, and #93) residents reviewed for accurate medical records. The Facility census
was 92.
Findings include:
1. Review of the medical record for Resident #26 revealed an admission date of 11/02/23. Diagnoses
included hemiplegia and hemiparesis following cerebral infarction affecting right dominant side, type II
diabetes mellitus, vascular dementia, hyperlipidemia, hypertension (HTN), symptomatic epilepsy and
epileptic syndrome, bipolar disorder, gastroesophageal reflux disease (GERD), and aphasia following
cerebral infarction.
Review of the most recent quarterly Minimum Data Set (MDS) assessment, dated 11/22/24, revealed a
Brief Interview of Mental Status (BIMS) score of 00, indicating Resident #26 was severely cognitively
impaired.
Review of the current physician orders for Resident #26 revealed an order dated 09/12/24 for Famotidine (a
medication used to treat ulcers of the stomach and intestine and prevent ulcers from coming back after they
have healed) oral suspension reconstituted 40 milligrams (mg) per 5 milliliters (ml). The order was to
administer 5 ml via PEG (a percutaneous endoscopic gastrostomy (PEG) tube is a tube that is surgically
placed into the stomach to allow a person to receive nutrition and medications when they are unable to
swallow orally) tube at bedtime for acid reflux.
Review of the medication administration record (MAR) for Resident #26 revealed the resident did not
receive the ordered 5 ml dose of Famotidine on 12/15/24, 12/19/24, 12/21/24, 12/22/24, and 12/24/24.
Review of the MAR for Resident #26 revealed the entry on 12/15/24 stated hold, see nurses note. Review
of the nurse progress note dated 12/15/24 for Resident #26 revealed Famotidine 5 ml was on order.
Review of the MAR for Resident #26 revealed the entry on 12/19/24 stated hold/see nurses note. Review of
the nurse progress notes for Resident #26 dated 12/19/24 revealed Famotidine 5 ml was documented as
not available.
Review of the MAR for Resident #26 revealed the entry on 12/21/24 stated hold/see nurses note.
(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 6
Event ID:
366022
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
366022
B. Wing
A. Building
(X3) DATE SURVEY
COMPLETED
01/14/2025
NAME OF PROVIDER OR SUPPLIER
STREET ADDRESS, CITY, STATE, ZIP CODE
Manor at Perrysburg
250 Manor Drive
Perrysburg, OH 43551
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 0755
Level of Harm - Minimal harm
or potential for actual harm
Residents Affected - Few
Review of the nurse progress notes for Resident #26 dated 12/21/24 revealed Famotidine 5 ml was
documented as on order.
Review of the MAR for Resident #26 revealed the entry on 12/22/24 stated hold/see nurses note. Review of
the nurse progress note for Resident #26 dated 12/22/24 revealed Famotidine 5 ml was documented as not
available.
Review of the MAR for Resident #26 revealed the entry on 12/24/24 stated hold/see nurses note. Review of
the nurse progress notes for Resident #26 dated 12/24/24 revealed Famotidine 5 ml was documented as
not available.
An interview with the Director of Nursing (DON) verified Resident #26 had not received the physician
ordered 5 ml dose of Famotidine on 12/15/24, 12/19/24, 12/21/24, 12/22/24, and 12/24/24 as the
medication was not available.
2. Review of the medical record for Resident #80 revealed an admission date of 12/11/2. Diagnoses
included hypothyroidism, diverticulitis of large intestine, hypokalemia, gastroesophageal reflux disease, and
hyperlipidemia.
Review of the MDS assessment, dated 12/29/24, revealed Resident #80 had a BIMS score of 11, indicating
moderate cognitive impairment.
Review of the current physician orders for Resident #80 revealed an order for Omeprazole (a medication
used to treat certain stomach and esophagus problems, such as acid reflux and ulcers) Delayed Release
20 mg with one capsule to be administered by mouth each morning for acid indigestion related to GERD.
Review of the medication administration record revealed Resident #80 had not receive the ordered dose of
Omeprazole Delayed Release capsule 20 mg on 12/13/24, 12/16/24, 12/18/24, and 12/19/24.
Review of the MAR for Resident #80 revealed the entry on 12/13/24 stated hold/see nurses note. Review of
the nurse progress note dated 12/13/24 revealed Omeprazole Delayed Release capsule 20 mg was
unavailable.
Review of the MAR for Resident #80 revealed the entry on 12/16/24 stated not required. Review of the
nurse progress notes for 12/16/24 revealed no documentation to support he documentation contained in
the MAR.
Review of the MAR for Resident #80 revealed the entry on 12/18/24 stated hold/see nurses note. Review of
the nurse progress note dated 12/18/24 revealed Omeprazole Delayed Release capsule 20 mg was out of
stock - on order.
Review of the MAR for Resident #80 revealed the entry on 12/19/24 stated hold/see nurses note. Review of
the nurse progress notes dated 12/19/24 revealed no note to support the documentation contained in the
MAR.
An interview with the DON verified Resident #80 had not received the physician ordered doses of the
Omeprazole Delayed Release capsule, 20 mg on the dates of 12/13/24, 12/16/24, 12/18/24, and 12/19/24.
(continued on next page)
FORM CMS-2567 (02/99)
Previous Versions Obsolete
Event ID:
Facility ID:
366022
If continuation sheet
Page 2 of 6
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
366022
B. Wing
A. Building
(X3) DATE SURVEY
COMPLETED
01/14/2025
NAME OF PROVIDER OR SUPPLIER
STREET ADDRESS, CITY, STATE, ZIP CODE
Manor at Perrysburg
250 Manor Drive
Perrysburg, OH 43551
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 0755
Level of Harm - Minimal harm
or potential for actual harm
Residents Affected - Few
Concurrent interview with the DON revealed there were no hold parameters outlined by the physician in the
Omeprazole Delayed Release capsule order that would constitute the medication to be documented as not
required on 12/16/24.
Review of the facility policy titled, Medication Administration - General Guidelines, with a revision date of
03/20/18 revealed medications are administered as prescribed in accordance with good nursing practices.
This deficiency represents non-compliance investigated under Complaint Number OH00161236.
FORM CMS-2567 (02/99)
Previous Versions Obsolete
Event ID:
Facility ID:
366022
If continuation sheet
Page 3 of 6
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
366022
B. Wing
A. Building
(X3) DATE SURVEY
COMPLETED
01/14/2025
NAME OF PROVIDER OR SUPPLIER
STREET ADDRESS, CITY, STATE, ZIP CODE
Manor at Perrysburg
250 Manor Drive
Perrysburg, OH 43551
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
Based on review of facility medical record, review, staff interview, and review of facility policy, the facility
failed to ensure that residents were free of significant mediation errors. This affected three residents (#26,
#89, and #93) of five residents (#26, #71, #80, #89, and #93) reviewed for accurate medical records. The
Facility census was 92.
Residents Affected - Few
Findings include:
1. Review of the medical record for Resident #26 revealed an admission date of 11/02/23. Diagnoses
included hemiplegia and hemiparesis following cerebral infarction affecting right dominant side, type II
diabetes mellitus, vascular dementia, hyperlipidemia, hypertension (HTN), symptomatic epilepsy and
epileptic syndrome, bipolar disorder, gastroesophageal reflux disease (GERD), and aphasia following
cerebral infarction.
Review of the most recent quarterly Minimum Data Set (MDS) assessment, dated 11/22/24, revealed a
Brief Interview of Mental Status (BIMS) score of 00, indicating Resident #26 was severely cognitively
impaired.
Further review of the current physician orders for Resident #26 revealed a physician order written on
11/07/23 for Novolog insulin, 100 units per milliliter (u/ml) to be injected subcutaneously (under the skin)
per a sliding scale every eight hours related to diabetes mellitus.
Review of the medication administration record for Resident #26 revealed the resident did not receive the
ordered sliding scale dose of Novolog on 12/02/24 at 10:00 P.M., on 12/03/24 at 6:00 A.M., and on
01/05/25 at 6:00 A.M.
An interview with the DON verified Resident #26 did not receive the ordered sliding scale dose of Novolog
on 12/02/24 at 10:00 P.M., on 12/03/24 at 6:00 A.M., and on 01/05/25 at 6:00 A.M.
2. Review of the medical record for Resident #89 revealed an admission date of 12/05/24. Diagnoses
included of aphasia (inability to speak) following cerebral infarction (stroke), and type II diabetes mellitus.
Review of the Medicare Five Day MDS assessment for Resident #89, dated 01/08/25 revealed a BIMS
score of 00, indicating Resident #89 was severely cognitively impaired.
Review of the current physician orders for Resident #89 revealed an order for 25 units of Lantus insulin 100
mg/ml to be injected subcutaneously two times a day for diabetes mellitus.
Review of the medication administration record for Resident #89 revealed the resident had not received the
ordered afternoon dose of 25 units of Lantus insulin, scheduled on 01/05/25 at 4:00 P.M.
An interview with the DON verified Resident #89 had not receive the ordered afternoon dose of 25 units of
Lantus on 01/05/25 at 4:00 P.M.
3. Review of the medical record for Resident #93 revealed an admission date of 09/30/23. Diagnoses
included type II diabetes mellitus, morbid obesity, major depressive disorder, and hypertension.
(continued on next page)
FORM CMS-2567 (02/99)
Previous Versions Obsolete
Event ID:
Facility ID:
366022
If continuation sheet
Page 4 of 6
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
366022
B. Wing
A. Building
(X3) DATE SURVEY
COMPLETED
01/14/2025
NAME OF PROVIDER OR SUPPLIER
STREET ADDRESS, CITY, STATE, ZIP CODE
Manor at Perrysburg
250 Manor Drive
Perrysburg, OH 43551
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
Review of the most recent quarterly MDS assessment for Resident #93, dated 10/18/24, revealed a BIMS
score of 15, indicating Resident #93 had intact cognition.
Review of the current physician orders for resident #93 revealed an order for 25 units of Insulin Glargine
Solution 100 mg per ml to be injected subcutaneously twice a day for diabetes mellitus.
Residents Affected - Few
Review of the MAR for Resident #93 revealed the resident had not receive the ordered morning dose of 25
units of Insulin Glargine on 12/22/24.
An interview with the Director of Nursing on 01/05/25 at 4:00 P.M. verified Resident #93 had not received
the ordered morning dose of 25 units of Insulin Glargine on 12/22/24.
Review of the facility policy titled, Medication Administration - General Guidelines, with a revision date of
03/20/18 revealed medications are administered as prescribed in accordance with good nursing practices.
This deficiency represents non-compliance investigated under Complaint Number OH00161236.
FORM CMS-2567 (02/99)
Previous Versions Obsolete
Event ID:
Facility ID:
366022
If continuation sheet
Page 5 of 6
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
366022
B. Wing
A. Building
(X3) DATE SURVEY
COMPLETED
01/14/2025
NAME OF PROVIDER OR SUPPLIER
STREET ADDRESS, CITY, STATE, ZIP CODE
Manor at Perrysburg
250 Manor Drive
Perrysburg, OH 43551
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, staff interview, medical record review, and review of facility policy, the facility failed to
ensure gloves were worn while administering subcutaneous insulin. This affected one resident (#71) of five
(#26, #71, #80, #89, and #93) reviewed for medication administration. The facility identified 24 residents
(#3, #4, #7, #8, #9, #10, #17, #26, #28, #29, #32, #39, #42, #50, #61, #65, #67, #69, #70, #71, #73, #79,
#89, and #93) who were prescribed insulin. The facility census was 92.
Residents Affected - Few
Findings include:
Review of the medical record for Resident #71 revealed an admission date of 02/18/23 with diagnoses of
hemiplegia and hemiparesis, and type two diabetes mellitus, type II.
Review of the current physician orders for Resident #71 revealed an order, dated 05/03/22, for 16 units of
Lantus SoloStar Solution Pen-injector 100 unit per milliliter (ml) to be administered subcutaneously
(injected under the skin) (SQ) one time a day for diabetes mellitus, type II.
Observation of medication administration to Resident #71 on 01/14/25 at 7:40 A.M. revealed Registered
Nurse (RN) #147 did not wear gloves while administering 16 units of Lantus SoloStar Solution Pen-injector
100 unit per ml to Resident #71.
Interview on 01/14/25 at 7:42 A.M. with RN #147 verified gloves were not worn when 16 units of Lantus
SoloStar Solution Pen-injector 100 unit per ml was administered to Resident #71.
Review of the facility policy titled, Gloves, with a revision date of 08/09/16, revealed all personnel must wear
gloves while performing a task that involves the potential exposure to blood or body fluids. Gloves shall be
worn when working with sharp items.
FORM CMS-2567 (02/99)
Previous Versions Obsolete
Event ID:
Facility ID:
366022
If continuation sheet
Page 6 of 6