F 0580
Level of Harm - Minimal harm
or potential for actual harm
Residents Affected - Few
Immediately tell the resident, the resident's doctor, and a family member of situations (injury/decline/room,
etc.) that affect the resident.
**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** Based on
medical record review, observation, staff interview, physician interview, review of pharmacy delivery sheets,
review of Controlled Drug Receipt/Records, and review of the facility policy, the facility failed to notify the
physician when residents were not administered medications as ordered by the physician. This affected one
(#75) out of the three residents reviewed for notification. The facility census was 61. Findings include:
Review of the medical record for Resident #75 revealed the resident was admitted to the facility on [DATE],
discharged on 08/12/25 and never returned. Diagnoses included dementia, anxiety disorder,
hypo-osmolality and hyponatremia, major depressive disorder, diabetes mellitus (DM), atrial fibrillation,
hypercholesterolemia, peripheral vascular disease, gastro-esophageal reflux disease, and hypothyroidism.
Review of the Minimum Data Set (MDS) assessment for Resident #75, dated 08/12/25, revealed the
resident was cognitively impaired and was dependent on staff for medication administration.Review of
physician orders for Resident #75 dated 07/08/25 and discontinued on 08/12/25, revealed the resident was
ordered Diltiazem (used to treat high blood pressure and heart rhythm disorders) extended release (ER)
180 milligrams (mg) daily in the morning, Sotalol (used to treat abnormal heart rhythms) 80 mg one half
tablet (40 mg) twice daily and oxycodone (narcotic pain reliever) five mg every six hours as needed (PRN)
for pain. Physician orders dated 07/19/25 and discontinued on 08/12/25, revealed the resident was ordered
to receive isosorbide mononitrate (vasodilator used to treat heart conditions) ER 30 mg every morning.
Physician orders dated 07/26/25 and discontinued on 08/02/25, revealed the resident was ordered
metformin 500 mg daily. Review of the July 2025 medication administration record (MAR) for Resident #75
revealed the following: a) From 07/22/25 through 07/31/25, it was documented that the resident received
diltiazem 180 mg daily, except for 07/28/25 (blank entry). b) From 07/24/25 through 07/31/25, it was
documented that the resident received sotalol 80 mg twice daily, except for the morning dose of 07/28/25
(blank entry). c) From 07/19/25 through 07/29/25, it was documented the resident received isosorbide 30
mg daily, except for 07/28/25 (blank entry). a) On 07/26/25, 07/27/25, 07/28/25 (blank entry) and 07/29/25,
the resident did not receive metformin 500 mg due to the medication being unavailable/new order. e) On the
morning of 07/28/25, Lasix (anti-diuretic) 40 mg, Eliquis (anti-coagulant), Lantus (insulin) 20 units,
cholecalciferol (vitamin D-3) (supplement), and lidocaine patch (pain reliever) were blank which indicated
the resident was not administered the medications. There was also no documented blood sugar check
(accuchecks) completed on 07/28/25 in the morning. Review of the August 2025 MAR for Resident #75
revealed the following: a) From 08/01/25 through 08/06/25, it was documented that the resident received
diltiazem 180 mg daily. The MAR indicated the resident did not receive diltiazem 180 mg on 08/07/25,
08/10/25 (blank entry), 08/11/25 and 08/12/25, due to the medication not being available. b) From 08/01/25
through 08/04/25, it was documented that the resident received sotalol 80 mg twice daily. c) On 08/03/25
and 08/12/24, the MAR indicated the resident did
(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 7
Event ID:
365974
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
365974
B. Wing
A. Building
(X3) DATE SURVEY
COMPLETED
10/07/2025
NAME OF PROVIDER OR SUPPLIER
STREET ADDRESS, CITY, STATE, ZIP CODE
Ohio Living Quaker Heights
514 West High Street
Waynesville, OH 45068
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 0580
Level of Harm - Minimal harm
or potential for actual harm
Residents Affected - Few
not receive isosorbide due to medication no being available. d) From 08/09/25 through 08/11/25, the MAR
was blank for oxycodone five mg, which indicated no medications were administered. Review of a progress
note for Resident #75 dated 08/12/25 at 9:59 A.M., revealed the resident presented with an altered mental
status (AMS) along with abnormal vital signs. The resident's pulse fluctuated between 29 and 40 beats per
minute (normal 60-80), blood pressure was 130 over 97 milliliters of mercury (mmHg), oxygen saturation
was 95 percent (%), and her body temperature was 97.9 Fahrenheit (F). Resident #75 was diaphoretic,
complained of numbness in her right arm and hand along with three episodes of emesis. The resident was
transferred to the hospital via squad. Review of the Prescription Order Status (a printed form by the facility
showing the medications ordered and delivered) for Resident #75 on 10/07/25 at 2:00 P.M., revealed the
resident had the following medications delivered to the facility: On 07/08/25, a quantity of 14 diltiazem 180
ER, a quantity of 14 sotalol 80 mg and a quantity of nine oxycodone five mg were delivered to the facility.
On 07/14/25, a quantity of 28 oxycodone five mg were delivered. On 07/29/25, a quantity of 14 isosorbide
30 mg ER were delivered. On 08/04/25 a quantity of 14 sotalol were delivered. On 08/06/25, a quantity of
14 Diltiazem 180 mg ER were delivered and on 08/12/25, a quantity of 14 isosorbide tablets were delivered
on 08/12/25. Review of a Controlled Drug Receipt/Record (Narcotic sheet) for Resident #75 75 on 10/07/25
at 2:10 P.M., revealed the facility received 28 oxycodone five mg tablets on 07/14/25. The resident was
administered oxycodone on a regular basis from 07/16/25 through 08/08/25 when the card was empty.
There were no additional oxycodone five mg received for Resident #75 after 08/08/25. Interview on
10/07/25 at 3:44 P.M. with the Director of Nursing (DON) confirmed the facility received 14 Diltiazem 180
mg for Resident #75 on 07/08/25, and 14 more 08/06/25. The DON verified Resident #75 was ordered to
receive diltiazem 180 mg daily from 07/08/25 through 08/12/25. The DON verified the resident's MAR
indicated the resident received diltiazem 180 mg from 07/22/25 through 08/06/25, despite the facility not
having the medications in the facility and stated she could not explain the discrepancy. The DON also
verified Resident #75 did not receive diltiazem 180 mg on 08/07/25, 08/10/25, and 08/11/25 due to the
MAR indicating the medication was not available. The DON also verified the facility received 14 sotalol 80
mg for Resident #75 on 07/08/25 and 14 more on 08/04/25. The DON verified Resident #75 was ordered to
receive sotalol 80 mg one half tablet twice daily from 07/08/25 through 08/12/25. The DON stated the 14
sotalol 80 mg received on 07/08/25 would have finished on 07/23/25. The DON verified the resident's MAR
indicated the resident received sotalol 80 one half tablet twice daily from 07/24/25 through 08/04/25,
despite the facility not having the sotalol in the facility and stated she could not explain the discrepancy. The
DON also verified the facility received 14 isosorbide 30mg for Resident #75 on 07/29/25 and 14 more on
08/12/25. The DON verified Resident #75 was ordered to receive isosorbide ER 30 mg daily from 07/19/25
through 08/12/25. The DON verified the resident's MAR indicated the resident received isosorbide 30 mg
from 07/19/25 through 07/29/25, despite the facility not having the medications in the facility and stated she
could not explain the discrepancy. The DON also verified the facility received eight oxycodone five mg for
Resident #75 on 07/08/25 and 28 more on 07/14/25. The DON verified Resident #75 received oxycodone
regularly from 07/09/25 through 08/08/25 The DON verified the oxycodone five mg was not available for
resident from 08/09/25 through 08/12/25. The DON stated a nurse requested a refill on 08/11/25 at 12:26
P.M. and the order was never filled. The DON stated she checked the facility's emergency supply box
(e-box) list, and it did not reveal any indications of the nursing staff removing diltiazem, isosorbide
mononitrate, sotalol, or oxycodone for Resident #75. The DON verified there was no documented evidence
that the physician was notified of Resident #75 medication discrepancies. The DON stated it was the
expectation for the nursing
(continued on next page)
FORM CMS-2567 (02/99)
Previous Versions Obsolete
Event ID:
Facility ID:
365974
If continuation sheet
Page 2 of 7
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
365974
B. Wing
A. Building
(X3) DATE SURVEY
COMPLETED
10/07/2025
NAME OF PROVIDER OR SUPPLIER
STREET ADDRESS, CITY, STATE, ZIP CODE
Ohio Living Quaker Heights
514 West High Street
Waynesville, OH 45068
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 0580
Level of Harm - Minimal harm
or potential for actual harm
Residents Affected - Few
FORM CMS-2567 (02/99)
Previous Versions Obsolete
staff to contact the physician for any missed medications.Interview on 10/07/25 at 10:49 A.M. with PCP
#500 stated he was never notified of the medication discrepancies for Resident #75. PCP #500 stated he
was concerned about the medication discrepancies because Resident #75 was discharged to the hospital
on [DATE] for heart related issues. Interview on 10/07/25 at 11:31 A.M. with Licensed Practical Nurse (LPN)
#181 who stated she does not notify the physician if a resident missed medications. LPN #181 stated she
would only notify the physician if the medication was an important medication but could not give an
example of what an important medication was.Review of a text message exchange between Primary Care
Physician (PCP) #500 and 100-200 hall nurse on 10/07/25 at 10:40 A.M. revealed the 100-200 hall nurse
sent a text message to PCP #500 on 08/11/25 at 12:26 P.M. and reported Resident #75 needed a new
script for PRN Oxycodone. At 4:09 P.M. the 100-200 hall nurse sent a text message to PCP #500 and noted
Resident #75 had several episodes of diarrhea and wanted to give the resident Imodium. PCP #500
responded with an order for Imodium four mg three times a day prn. The message did not include anything
about the oxycodone refill. Review of the facility policy titled Notification of Change dated 09/14/23
confirmed notifications of changes will be completed and documented. An immediate notification of the
resident's physician will be completed for a need to alter treatments.
Event ID:
Facility ID:
365974
If continuation sheet
Page 3 of 7
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
365974
B. Wing
A. Building
(X3) DATE SURVEY
COMPLETED
10/07/2025
NAME OF PROVIDER OR SUPPLIER
STREET ADDRESS, CITY, STATE, ZIP CODE
Ohio Living Quaker Heights
514 West High Street
Waynesville, OH 45068
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 0677
Provide care and assistance to perform activities of daily living for any resident who is unable.
Level of Harm - Minimal harm
or potential for actual harm
**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** Based on
medical record review, the facility staff interview, and facility policy review the facility failed to provide
resident with showers. This affected one (#75) out of the three residents reviewed for showers. The facility
census was 61.Findings include:Review of the medical record for Resident #75 revealed she was admitted
to the facility on [DATE]. Resident #75 was discharged to the hospital on [DATE] and never returned.
Diagnoses included anxiety disorder, hypo-osmolality and hyponatremia, major depressive disorder,
diabetes mellitus (DM), atrial fibrillation, hypercholesterolemia, peripheral vascular disease,
gastro-esophageal reflux disease, and hypothyroidism. Review of the July 2025 shower/bathing sheets for
Resident #75, revealed the resident was documented as only receiving a shower on 07/14/25 and
07/24/25. Resident #75 had no documented showers for August 2025. Review of the Minimum Data Set
(MDS) assessment for Resident #75, dated 08/12/25, revealed her cognitive status was not assessed and
the resident was dependent on staff for personal hygiene and bathing/showers. Interview with the Director
of Nursing (DON) on 10/07/25 at 3:44 P.M. who stated the residents were assigned two shower/bathing
days a week and more if needed or requested. The DON verified Resident #75 only received a shower on
07/14/25 and 07/24/25, and there was no documented evidence Resident #75 received any
showers/bathing in August 2025. Review of the facility policy titled Bathing dated 02/04/24 revealed the
purpose of the bathing policy was to ensure residents receive bathing and given choices if desired. Further
review of the policy revealed the residents were scheduled for bathing two times per week.This deficiency
represents non-compliance investigated under Complaint Number 2625070.
Residents Affected - Few
FORM CMS-2567 (02/99)
Previous Versions Obsolete
Event ID:
Facility ID:
365974
If continuation sheet
Page 4 of 7
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
365974
B. Wing
A. Building
(X3) DATE SURVEY
COMPLETED
10/07/2025
NAME OF PROVIDER OR SUPPLIER
STREET ADDRESS, CITY, STATE, ZIP CODE
Ohio Living Quaker Heights
514 West High Street
Waynesville, OH 45068
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
medical record review, observation, staff interview, physician interview, review of pharmacy delivery sheets,
review of Controlled Drug Receipt/Records, and review of the facility policy, the facility failed to ensure
residents were free of significant medication errors. This affected one (#75) of the three residents reviewed
for medications. The census was 57. Findings include: Review of the medical record for Resident #75
revealed the resident was admitted to the facility on [DATE], discharged on 08/12/25 and never returned.
Diagnoses included dementia, anxiety disorder, hypo-osmolality and hyponatremia, major depressive
disorder, diabetes mellitus (DM), atrial fibrillation, hypercholesterolemia, peripheral vascular disease,
gastro-esophageal reflux disease, and hypothyroidism. Review of the Minimum Data Set (MDS)
assessment for Resident #75, dated 08/12/25, revealed the resident was cognitively impaired and was
dependent on staff for medication administration.Review of physician orders for Resident #75 dated
07/08/25 and discontinued on 08/12/25, revealed the resident was ordered Diltiazem (used to treat high
blood pressure and heart rhythm disorders) extended release (ER) 180 milligrams (mg) daily in the
morning, Sotalol (used to treat abnormal heart rhythms) 80 mg one half tablet (40 mg) twice daily and
oxycodone (narcotic pain reliever) five mg every six hours as needed (PRN) for pain. Physician orders
dated 07/19/25 and discontinued on 08/12/25, revealed the resident was ordered to receive isosorbide
mononitrate (vasodilator used to treat heart conditions) ER 30 mg every morning. Physician orders dated
07/26/25 and discontinued on 08/02/25, revealed the resident was ordered metformin 500 mg daily. Review
of the progress notes for Resident #75 from 07/22/25 through 08/11/25, revealed no documentation of the
physician being notified of the medication discrepancies. Review of the July 2025 medication administration
record (MAR) for Resident #75 revealed the following: a) From 07/22/25 through 07/31/25, it was
documented that the resident received diltiazem 180 mg daily, except for 07/28/25 (blank entry). b) From
07/24/25 through 07/31/25, it was documented that the resident received sotalol 80 mg twice daily, except
for the morning dose of 07/28/25 (blank entry). c) From 07/19/25 through 07/29/25, it was documented the
resident received isosorbide 30 mg daily, except for 07/28/25 (blank entry). d) On 07/26/25, 07/27/25,
07/28/25 (blank entry) and 07/29/25, the resident did not receive metformin 500 mg due to the medication
being unavailable/new order. e) On the morning of 07/28/25, Lasix (anti-diuretic) 40 mg, Eliquis
(anti-coagulant), Lantus (insulin) 20 units, cholecalciferol (vitamin D-3) (supplement), and lidocaine patch
(pain reliever) were blank which indicated the resident was not administered the medications. There was
also no documented blood sugar check (accuchecks) completed on 07/28/25 in the morning. Review of the
August 2025 MAR for Resident #75 revealed the following: a) From 08/01/25 through 08/06/25, it was
documented that the resident received diltiazem 180 mg daily. The MAR indicated the resident did not
receive diltiazem 180 mg on 08/07/25, 08/10/25 (blank entry), 08/11/25 and 08/12/25, due to the
medication not being available. b) From 08/01/25 through 08/04/25, it was documented that the resident
received sotalol 80 mg twice daily. c) On 08/03/25 and 08/12/24, the MAR indicated the resident did not
receive isosorbide due to medication no being available. d) from 08/09/25 through 08/11/25, the MAR was
blank for oxycodone five mg, which indicated no medications were administered. Review of a progress note
for Resident #75 dated 08/12/25 at 9:59 A.M., revealed the resident presented with an altered mental
status (AMS) along with abnormal vital signs. The resident's pulse fluctuated between 29 and 40 beats per
minute (normal 60-80), blood pressure was 130 over 97 milliliters of mercury (mmHg), oxygen saturation
was 95 percent (%), and her body temperature was 97.9 Fahrenheit (F). Resident #75 was diaphoretic,
complained of numbness in her right arm and hand along with three episodes of emesis. The resident was
transferred to the hospital via
Residents Affected - Few
(continued on next page)
FORM CMS-2567 (02/99)
Previous Versions Obsolete
Event ID:
Facility ID:
365974
If continuation sheet
Page 5 of 7
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
365974
B. Wing
A. Building
(X3) DATE SURVEY
COMPLETED
10/07/2025
NAME OF PROVIDER OR SUPPLIER
STREET ADDRESS, CITY, STATE, ZIP CODE
Ohio Living Quaker Heights
514 West High Street
Waynesville, OH 45068
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
squad. Review of the Prescription Order Status (a printed form by the facility showing the medications
ordered and delivered) for Resident #75 on 10/07/25 at 2:00 P.M., revealed the resident had the following
medications delivered to the facility: On 07/08/25, a quantity of 14 diltiazem 180 ER, a quantity of 14 sotalol
80 mg and a quantity of nine oxycodone five mg were delivered to the facility. On 07/14/25, a quantity of 28
oxycodone five mg were delivered. On 07/29/25, a quantity of 14 isosorbide 30 mg ER were delivered. On
08/04/25 a quantity of 14 sotalol were delivered. On 08/06/25, a quantity of 14 Diltiazem 180 mg ER were
delivered and on 08/12/25, a quantity of 14 isosorbide tablets were delivered on 08/12/25. Review of a
Controlled Drug Receipt/Record (Narcotic sheet) for Resident #75 75 on 10/07/25 at 2:10 P.M., revealed
the facility received 28 oxycodone five mg tablets on 07/14/25. The resident was administered oxycodone
on a regular basis from 07/16/25 through 08/08/25 when the card was empty. There were no additional
oxycodone five mg received for Resident #75 after 08/08/25. Interview on 10/07/25 at 3:44 P.M. with the
Director of Nursing (DON) confirmed the facility received 14 Diltiazem 180 mg for Resident #75 on
07/08/25, and 14 more 08/06/25. The DON verified Resident #75 was ordered to receive diltiazem 180 mg
daily from 07/08/25 through 08/12/25. The DON verified the resident's MAR indicated the resident received
diltiazem 180 mg from 07/22/25 through 08/06/25, despite the facility not having the medications in the
facility and stated she could not explain the discrepancy. The DON also verified Resident #75 did not
receive diltiazem 180 mg on 08/07/25, 08/10/25, and 08/11/25 due to the MAR indicating the medication
was not available. The DON also verified the facility received 14 sotalol 80 mg for Resident #75 on 07/08/25
and 14 more on 08/04/25. The DON verified Resident #75 was ordered to receive sotalol 80 mg one half
tablet twice daily from 07/08/25 through 08/12/25. The DON stated the 14 sotalol 80 mg received on
07/08/25 would have finished on 07/23/25. The DON verified the resident's MAR indicated the resident
received sotalol 80 one half tablet twice daily from 07/24/25 through 08/04/25, despite the facility not having
the sotalol in the facility and stated she could not explain the discrepancy. The DON also verified the facility
received 14 isosorbide 30mg for Resident #75 on 07/29/25 and 14 more on 08/12/25. The DON verified
Resident #75 was ordered to receive isosorbide ER 30 mg daily from 07/19/25 through 08/12/25. The DON
verified the resident's MAR indicated the resident received isosorbide 30 mg from 07/19/25 through
07/29/25, despite the facility not having the medications in the facility and stated she could not explain the
discrepancy. The DON also verified the facility received eight oxycodone five mg for Resident #75 on
07/08/25 and 28 more on 07/14/25. The DON verified Resident #75 received oxycodone regularly from
07/09/25 through 08/08/25 The DON verified the oxycodone five mg was not available for resident from
08/09/25 through 08/12/25. The DON stated a nurse requested a refill on 08/11/25 at 12:26 P.M. and the
order was never filled. The DON stated she checked the facility's emergency supply box (e-box) list, and it
did not reveal any indications of the nursing staff removing diltiazem, isosorbide mononitrate, sotalol, or
oxycodone for Resident #75. Interview on 10/07/25 at 10:49 A.M. with PCP #500 stated he was never
notified of the medication discrepancies for Resident #75. PCP #500 stated he was concerned about the
medication discrepancies because Resident #75 was discharged to the hospital on [DATE] for heart related
issues. Review of a text message exchange between Primary Care Physician (PCP) #500 and 100-200 hall
nurse on 10/07/25 at 10:40 A.M. revealed the 100-200 hall nurse sent a text message to PCP #500 on
08/11/25 at 12:26 P.M. and reported Resident #75 needed a new script for PRN Oxycodone. At 4:09 P.M.
the 100-200 hall nurse sent a text message to PCP #500 and noted Resident #75 had several episodes of
diarrhea and wanted to give the resident Imodium. PCP #500 responded with an order for Imodium four mg
three times a day prn. The message did not include anything about the oxycodone refill. Review of the
undated facility policy titled Medication
(continued on next page)
FORM CMS-2567 (02/99)
Previous Versions Obsolete
Event ID:
Facility ID:
365974
If continuation sheet
Page 6 of 7
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
365974
B. Wing
A. Building
(X3) DATE SURVEY
COMPLETED
10/07/2025
NAME OF PROVIDER OR SUPPLIER
STREET ADDRESS, CITY, STATE, ZIP CODE
Ohio Living Quaker Heights
514 West High Street
Waynesville, OH 45068
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
Administration, revealed all medications would be administered in an organized, accurate and safe manner,
accordance with manufacturers specifications, and good nursing principles and practices. If a regularly
scheduled medication was withheld, refused or given at other than the scheduled time, the nurse shall
document in the MAR and enter an explanatory note in the record.
Residents Affected - Few
FORM CMS-2567 (02/99)
Previous Versions Obsolete
Event ID:
Facility ID:
365974
If continuation sheet
Page 7 of 7