F 0578
Level of Harm - Minimal harm
or potential for actual harm
Residents Affected - Few
Honor the resident's right to request, refuse, and/or discontinue treatment, to participate in or refuse to
participate in experimental research, and to formulate an advance directive.
**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** Based on
electronic and paper medical record review, staff interview, and review of the facility policy, the facility failed
to ensure accurate advanced directives were located in each medical record. This affected one (#13) of one
resident reviewed for advanced directives. The facility census was 51.
Findings include:
Review of Resident #13's medical record revealed an admission date of 07/22/21. Diagnoses included
dementia, hypertension, atherosclerotic heart disease, anxiety disorder, and depression.
Review of the quarterly Minimum Data Set (MDS) assessment dated [DATE] revealed Resident #13 was
severely cognitively impaired.
Review of a Do Not Resuscitate (DNR) Order Form dated 09/01/22, and located in Resident #13's paper
medical record, revealed the resident's advanced directives were DNR Comfort Care (meaning the DNR
protocol was effective immediately).
Review of a current physician order dated 07/31/23, and located in the electronic medical record (EMR)
revealed Resident #13's advanced directives were Do Not Resuscitate Comfort Care-Arrest (DNRCC-A),
meaning providers will treat the resident as any other without a DNR order until the point of cardiac or
respiratory arrest at which point all life saving interventions will stop and the DNR Comfort Care protocol
will be implemented.
Interview on 08/31/23 at 12:14 P.M. with Registered Nurse (RN) #510 stated staff members could check
either the paper chart or the EMR to determine a resident's advanced directives, if needed. RN #510
verified Resident #13's advanced directives order in the EMR did not match the order in the the paper
chart, and stated she would take care of it.
Review of an undated facility policy titled, Advance Directives, revealed documentation of advanced
directives will be maintained by the facility in the resident's current chart throughout the course of the stay.
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:
366097
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
366097
B. Wing
A. Building
(X3) DATE SURVEY
COMPLETED
08/31/2023
NAME OF PROVIDER OR SUPPLIER
STREET ADDRESS, CITY, STATE, ZIP CODE
Fulton Manor Nursing & Rehab C
723 South Shoop Avenue
Wauseon, OH 43567
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, observation, and staff interview, the facility failed to ensure a dependent resident
received adequate assistance with shaving. This affected one (#13) of one residents reviewed for activities
of daily living. The facility census was 51.
Residents Affected - Few
Findings include:
Review of Resident #13's medical record revealed an admission date of 07/22/21. Diagnoses included
dementia, hypertension, atherosclerotic heart disease, anxiety disorder, and depression.
Review of the quarterly Minimum Data Set (MDS) assessment dated [DATE] revealed Resident #13 was
severely cognitively impaired and required extensive assistance with personal hygiene.
Review of the plan of care initiated 08/13/21 revealed Resident #13 required assistance with activities of
daily living (ADLs) due to physical limitations secondary to dementia and anxiety. Interventions included to
set up supplies needed to assist with completion of ADLs, provide needed assistance of one staff member
for proper completion of ADLs, encourage the resident to do as much as possible for herself, and give
simple direct steps and allow ample time to complete the task at hand.
Observations on 08/29/23 at 8:12 A.M. and on 08/30/23 at 8:05 A.M. of Resident #13 revealed the resident
had several long hairs on her chin, approximately one-quarter inch in length.
Interview on 08/30/23 at 9:26 A.M. with State Tested Nurse Aide (STNA) #504 stated Resident #13 required
staff assistance with hygiene and grooming. STNA #504 stated shaving was typically done on shower days
and she assisted Resident #13 with a shower on 08/29/23. STNA #504 stated she did not shave residents
who did not have an electric razor because she was afraid of disposable razors. STNA #504 verified the
hair growth on Resident #13's chin and confirmed she did not assist the resident with shaving during her
shower on 08/29/23.
FORM CMS-2567 (02/99)
Previous Versions Obsolete
Event ID:
Facility ID:
366097
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
366097
B. Wing
A. Building
(X3) DATE SURVEY
COMPLETED
08/31/2023
NAME OF PROVIDER OR SUPPLIER
STREET ADDRESS, CITY, STATE, ZIP CODE
Fulton Manor Nursing & Rehab C
723 South Shoop Avenue
Wauseon, OH 43567
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 0686
Provide appropriate pressure ulcer care and prevent new ulcers from developing.
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 and staff interview, the facility failed to provide treatment for pressure ulcers per
physician order. This affected one (#7) of one residents reviewed for pressure ulcers. The facility identified
four residents with pressure ulcers. The facility census was 51.
Residents Affected - Few
Findings include:
Review of Resident #7's medical record revealed an admission date of 05/26/21. Diagnoses included
atherosclerosis of native arteries of extremities, hypotension, atrial fibrillation, type II diabetes chronic
kidney disease, chronic obstructive pulmonary disease (COPD), and major depressive disorder.
Review of the quarterly Minimum Data Set (MDS) assessment dated [DATE] revealed Resident #7 was
cognitively intact, was at risk for pressure ulcers, and had one stage II pressure ulcer (partial-thickness skin
loss with exposed dermis).
Review of the plan of care dated 06/07/21 revealed Resident #7 was at risk for skin breakdown.
Interventions included wound treatment per facility protocol or wound care.
Review of a wound care note dated 07/03/23 revealed Resident #7 had a stage II pressure wound to the
coccyx which was acquired on 05/11/23. Additional review of wound care notes dated 07/10/23, 07/17/23,
07/24/23, and 08/01/23 revealed no worsening of the wound, and Resident #7 refused to lay down during
the day to reduce pressure.
Review of an assessment used to predict pressure ulcer development dated 08/12/23 revealed Resident #7
was at moderate risk for pressure sores.
Review of physician orders dated 06/20/23 revealed Resident #7 was ordered to cleanse the sacral area
with normal saline, pat dry, pack the wound with a thin strip of Mesalt, cover with Allevyn dressing, and
change daily and as needed.
Review of Resident #7's treatment administration record (TAR) for July 2023 revealed sacral treatments
were not documented as provided on 07/04/23, 07/06/23, 07/11/23, 07/13/23, 07/18/23, 07/19/23,
07/20/23, and 07/22/23.
Interview on 08/29/23 at 3:58 P.M. with the Director of Nursing (DON) verified the facility had no evidence
Resident #7's wound treatments were administered as ordered by the physician on 07/04/23, 07/06/23,
07/11/23, 07/13/23, 07/18/23, 07/19/23, 07/20/23, and 07/22/23.
Interview on 08/30/23 at 8:59 A.M. with Licensed Practical Nurse (LPN) #505 stated she was the treatment
nurse. LPN #505 stated while Resident #7 was not always compliant with repositioning to relieve pressure,
the resident was compliant with wound treatments.
FORM CMS-2567 (02/99)
Previous Versions Obsolete
Event ID:
Facility ID:
366097
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
366097
B. Wing
A. Building
(X3) DATE SURVEY
COMPLETED
08/31/2023
NAME OF PROVIDER OR SUPPLIER
STREET ADDRESS, CITY, STATE, ZIP CODE
Fulton Manor Nursing & Rehab C
723 South Shoop Avenue
Wauseon, OH 43567
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 0695
Provide safe and appropriate respiratory care for a resident when needed.
Level of Harm - Minimal harm
or potential for actual harm
**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** Based on
observation, medical record review, staff interview, and review of facility policy, the facility failed to ensure a
resident receiving supplemental oxygen therapy had a physician order for use. This affected one (#301) of
residents reviewed for oxygen therapy. The facility identified nine residents that use supplemental oxygen.
The facility census was 51.
Residents Affected - Few
Findings include:
Review of the medical record for Resident #301 revealed an admission date of 08/23/23 with diagnoses of
heart failure and atrial fibrillation.
Review of an initial assessment dated [DATE] revealed the resident was alert and oriented to person, place,
and time, and was noted to have supplemental oxygen at two liters per minute by way of nasal cannula.
Review of Resident #301's current physician orders for August 2023 revealed there were not any orders for
supplemental oxygen therapy.
Observation on 08/28/23 at 3:26 P.M. revealed Resident #301 was resting in bed after lunch and therapy
with supplemental oxygen on at two liters per minute via nasal cannula.
Interview on 08/28/23 at 3:26 P.M. with Resident #301 stated she was on oxygen at home only in the
afternoon and during the night.
Observation on 08/29/23 at 7:45 A.M. revealed Resident #301 was resting in bed with supplemental oxygen
in place via nasal cannula at two liters per minute.
Observation on 08/31/23 at 8:04 A.M. revealed Resident #301 was sitting in her recliner eating breakfast
with supplemental oxygen on via nasal cannula at two liters per minute.
Interview on 08/31/23 at 8:05 A.M. with Registered Nurse (RN) #508 verified Resident #301 was receiving
supplemental oxygen by nasal cannula at two liters per minutes, and verified the medical record for
Resident #301 contained no orders for supplemental oxygen therapy.
Review of an undated facility policy titled, Oxygen Use/Administration, revealed oxygen must be prescribed
by a physician, and a complete order must be obtained to include liter flow per minute, titration instructions,
and type of delivery device (nasal cannula, simple mask).
FORM CMS-2567 (02/99)
Previous Versions Obsolete
Event ID:
Facility ID:
366097
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
366097
B. Wing
A. Building
(X3) DATE SURVEY
COMPLETED
08/31/2023
NAME OF PROVIDER OR SUPPLIER
STREET ADDRESS, CITY, STATE, ZIP CODE
Fulton Manor Nursing & Rehab C
723 South Shoop Avenue
Wauseon, OH 43567
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
Provide pharmaceutical services to meet the needs of each resident and employ or obtain the services of a
licensed pharmacist.
**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** Based on
medical record review, resident and staff interview, pharmacy staff interview, and review of a facility policy,
the facility failed to ensure medications were administered per physician order. This affected one (#39) of
three residents reviewed for medication administration. The facility census was 51.
Findings include:
Review of Resident #39's medical record revealed an admission date of 01/31/23. Diagnoses included
chronic obstructive pulmonary disease (COPD), hypertension, osteoarthritis, and repeated falls.
Review of the quarterly Minimum Data Set (MDS) assessment dated [DATE] revealed Resident #39 was
severely cognitively impaired.
Review of the plan of care initiated 02/20/23 revealed Resident #39 was at risk for shortness of breath
related to COPD. Interventions included to administer medications as ordered and monitor for adverse side
effects.
Review of a current physician order dated 07/13/23 revealed Resident #39 was ordered the combination
inhaled medication to treat COPD Breztri Aerosphere to receive two puffs orally two times a day.
Review of Resident #39's medication administration record (MAR) from 08/01/23 through 08/30/23 revealed
Breztri Aerosphere was documentated on 08/07/23 at the evening dose, on 08/08/23 at the morning dose,
on 08/09/23 at the evening dose, on 08/11/23 at the evening dose, on 08/12/23 at the morning dose, on
08/28/23 at the evening dose, and on 08/29/23 at the morning dose with the MAR code of 9. Further review
of the MAR revealed the code 9 indicated the medication was unavailable.
Review of Resident #39's nursing progress notes related to administration of Breztri Aerosphere revealed
on 08/07/23 the facility was waiting on pharmacy, on 08/08/23 the medication was on order, on 08/09/23
the medication was not available from pharmacy, on 08/11/23 the medication was not available, on
08/12/23 the medication was on order, and on 08/28/23 the medication was not available pharmacy was
called.
Interview on 08/28/23 at 12:27 P.M., with Resident #39 stated he had not received his Breztri Aerosphere
inhaler as physician ordered. Resident #39 stated nursing staff told him it had been ordered, but the
pharmacy had not delivered it. Resident #39 stated he was concerned he did not have his medication like
he was supposed to because he had blood clots in his lungs in the past.
Interview on 08/30/23 at 3:46 P.M., with the Director of Nursing (DON) verified Resident #39 did not receive
Breztri Aerosphere as ordered on 08/08/23, 08/09/23, 08/11/23, 08/12/23, and 08/28/23. The DON stated
she became aware on 08/28/23 the inhaler was not available, and it was believed it was accidentally thrown
away. The DON stated the medication was reordered on 08/28/23, but it was too early to refill the
medication. As a result, the DON authorized the refill with the facility paying for the cost of the medication.
The DON verified the medication should have been in the facility for administration, and Resident #39 did
not receive the inhaler as ordered.
Interview on 08/30/23 at 3:55 P.M., with Pharmacy Order Entry Technician (POET) #507 confirmed
(continued on next page)
FORM CMS-2567 (02/99)
Previous Versions Obsolete
Event ID:
Facility ID:
366097
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
366097
B. Wing
A. Building
(X3) DATE SURVEY
COMPLETED
08/31/2023
NAME OF PROVIDER OR SUPPLIER
STREET ADDRESS, CITY, STATE, ZIP CODE
Fulton Manor Nursing & Rehab C
723 South Shoop Avenue
Wauseon, OH 43567
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
Resident #39's Breztri Aerosphere was filled and delivered to the facility on [DATE] and 08/13/23. On
08/28/23, the pharmacy received a refill request but since each order was a 30-day supply, it was too soon
to fill the order request. POET #507 confirmed the facility authorized payment and the medication was
delivered on 08/29/23.
Review of an undated facility policy titled, Medication Administration Policy, revealed medications shall be
administered only upon the order of a physician or other Licensed Independent Practitioner who is
authorized to provide care to the resident. If a medication is not available during the process, the nurse
indicates this in the electronic medication administration record (EMAR). Additionally, a note is documented
in the EMAR by the nurse detailing the communication to the pharmacy regarding the missing medication.
This deficiency represents non-compliance investigated under Complaint Number OH00131350.
FORM CMS-2567 (02/99)
Previous Versions Obsolete
Event ID:
Facility ID:
366097
If continuation sheet
Page 6 of 6