F 0690
Level of Harm - Minimal harm
or potential for actual harm
Residents Affected - Few
Provide appropriate care for residents who are continent or incontinent of bowel/bladder, appropriate
catheter care, and appropriate care to prevent urinary tract infections.
**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** Based on
observation, medical record review, and resident and staff interview, the facility failed to ensure suprapubic
urinary catheter dressing changes were completed as ordered. This affected one (#32) of three residents
reviewed for dressing changes. The facility census was 44.
Findings include:
Review of Resident #32's medical record revealed admission to the facility occurred on 06/29/23.
Diagnoses included chronic obstructive pulmonary disease (COPD), anxiety, chronic kidney disease (CKD),
and obstructive uropathy.
Review of Resident #32's most recent Minimum Data Set (MDS) assessment dated [DATE] revealed
Resident #32 was assessed as cognitively intact and had a suprapubic urinary catheter in place.
Review of Resident #32's February 2023 physician orders revealed nursing staff should clean the urinary
catheter site and apply a sponge daily.
Interview and observation of Resident #32 on 02/07/23 at 9:45 A.M. stated the dressing to her suprapubic
urinary catheter was not changed the previous day. Resident #32 proceeded to lift her shirt and revealed
the dressing in place was not dated. Further observation of the dressing revealed there were no staff
initials, no time or date when the dressing was applied, and the dressing contained a large amount of
brown-colored drainage.
Observation of Resident #32's suprapubic urinary catheter dressing was completed with the Director of
Nursing (DON) on 02/07/24 at 9:55 A.M. The DON observed the dressing that was in place and confirmed
there was no date as to when the dressing was applied. Resident #32 stated to the DON at the time of the
observation that her dressing was not changed yesterday.
Interview on 02/07/24 at 9:55 A.M., with the DON at the time of the observation of Resident #32's dressing,
confirmed all dressings should have the date and nurses initials when it was applied. The DON also
confirmed Resident #32's dressing was noted with a large amount of brown drainage and confirmed the
dressing was not initialed or dated.
This deficiency represents non-compliance investigated under Master Complaint OH00150540.
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:
365911
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
365911
B. Wing
A. Building
(X3) DATE SURVEY
COMPLETED
02/07/2024
NAME OF PROVIDER OR SUPPLIER
STREET ADDRESS, CITY, STATE, ZIP CODE
Winchester Terrace
70 Winchester Rd
Mansfield, OH 44907
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 0919
Make sure that a working call system is available in each resident's bathroom and bathing area.
Level of Harm - Minimal harm
or potential for actual harm
**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** Based on
observation, review of maintenance repair logs, review of Resident Council meeting minutes, staff interview,
Ombudsman interview, and review of manufacturer instructions, the facility failed to ensure processes were
in place to ensure the resident call light system was tested and maintained in a fully functioning manner,
and staff had required equipment to be alerted to resident call lights. This had the potential to affect all 44
residents residing in the facility. The census was 44.
Residents Affected - Many
Findings include:
Review of the facility maintenance repair log for the past three months revealed on 11/12/23 both call lights
in room [ROOM NUMBER] were broken, the call light was broken in room [ROOM NUMBER], and the call
light in room [ROOM NUMBER] would not go off. On 11/15/23 the call light in room [ROOM NUMBER] and
in room [ROOM NUMBER], and in room [ROOM NUMBER]'s bathroom were not working. On 01/03/24 the
call light was not working in room [ROOM NUMBER], room [ROOM NUMBER], and room [ROOM
NUMBER].
Review of Resident Council meeting minutes dated 11/02/23 revealed call light system concerns were
voiced, and review of Resident Council meeting minutes dated 12/28/23 revealed the call light system was
replaced.
Interview with Assistant Director of Nursing (ADON) #45 on 02/07/23 at 7:18 A.M. confirmed the facility call
light system used pagers that staff members carried during their shift. The call light signal go to the pager
and that was how staff are notified when a resident activated their call light. ADON #45 confirmed when
agency staff work they are not provided a pager because as they kept leaving the facility with the pagers.
ADON #45 stated there was a computer screen at the Oak Hill nursing station that also listed when call
lights were activated. ADON #45 stated the staff can come to the Oak Hill nursing station to see when lights
are activated.
Interview and observation with Registered Nurse (RN) #31 occurred on 02/07/23 at 7:20 A.M. confirmed
she recently started working a the facility a few weeks ago. RN #31 confirmed she was not provided a
pager and verified she did not currently have one in her possession. RN #31 confirmed if she was on the
other side of the facility there was no way for her to know a resident activated their call light and needed
assistance.
Interview with State Tested Nurse Aide (STNA) #15 was completed on 02/07/24 at 7:23 A.M. and confirmed
agency staff members do not receive a pager to be notified if residents call for assistance when they work.
STNA #15 was not aware how staff members who worked on the other side of the facility would know when
residents activated their call lights.
Interview with the facility Ombudsman occurred on 02/07/24 at 9:33 A.M. confirmed there were concerns
the facility call light system was not working properly, and there were concerns from residents wondering if
staff knew when the residents activated their call lights.
Observation of the facility call light system was completed with Maintenance Director (MD) #36 and the
Director of Nursing (DON) on 02/07/24 a 1:35 P.M. A random check of the call light functionality was
completed and noted room [ROOM NUMBER], room [ROOM NUMBER] and room [ROOM NUMBER]'s call
lights were not functioning properly. room [ROOM NUMBER] was noted to illuminate the call box located in
the room; however, the signal was not going to the pager system. room [ROOM NUMBER]'s call light was
(continued on next page)
FORM CMS-2567 (02/99)
Previous Versions Obsolete
Event ID:
Facility ID:
365911
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
365911
B. Wing
A. Building
(X3) DATE SURVEY
COMPLETED
02/07/2024
NAME OF PROVIDER OR SUPPLIER
STREET ADDRESS, CITY, STATE, ZIP CODE
Winchester Terrace
70 Winchester Rd
Mansfield, OH 44907
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 0919
Level of Harm - Minimal harm
or potential for actual harm
Residents Affected - Many
pressed and the activation string pulled, but the call light did not activate. The box did not illuminate and no
signal was sent to the pager. room [ROOM NUMBER]'s call light was not functioning when tested. The
observations were confirmed in interview with MD #36 and the DON.
Interview with MD #36 and the DON, at the time of the observation, confirmed the resident room call boxes
frequently needed batteries replaced, and the call system should sent alerts to the computer when the
boxes are getting low battery signals.
Observation of the call light computer screen located at the Oak Hill nursing station on 02/07/24 at 1:53
P.M. revealed the screen was noted to include 23 alerts dating back to 02/02/24. The alerts identified low
battery and missing device. The missing device alerts were noted on the screen dated 02/02/24 for Rooms
#16, #18, #19, #37, #40, #41, #54, #71, #72, #73, #76, and #79. The computer also listed nine alerts dated
02/07/24 for low batteries for Rooms #18, #19, #20, #33, #37, #40, #41, #76, and #79.
Interview with MD #36 and the DON, at the time of the observation on 02/07/24 at 1:53 P.M., stated no one
was currently in charge of fixing call light system alerts or checking the status of the alerts. Interview with
MD #36 and the DON confirmed they did not really know what some of the alerts on the call system were
or what the alerts meant.
Observation and interview with MD #36 on 02/07/24 at 1:53 P.M. revealed MD #36 brought the call light box
from room [ROOM NUMBER] and opened the box. MD #36 stated sometimes when the boxes were
dropped something inside the box breaks loose and will illuminate; however, it will not send a signal to the
pagers. MD #36 confirmed residents could think they activated their call light when in reality the signal was
not being sent to the pagers. MD #36 confirmed the facility has no documented evidence of any ongoing
testing of the call light system. MD #36 stated the issue with the call light boxes not sending a signal
occurred a lot, and confirmed he needed to fix the boxes or replace the batteries almost daily. MD #36
stated in December 2023 the computer system for the call light system was replaced, because the entire
system went down, but there was no evidence of him being trained on how to maintain the new call light
system.
Review of the facility call light system manufactures instruction contained an undated form letter that
revealed a footprint test of the system was vitally important to be completed at least weekly. The
instructions further revealed when using a pendent, send a test alarm from each of your test points and
then validate that your call has registered on the Arial® computer and/or a pager carried by staff. Also,
record your test results so that you will know if any system variances occur. Failure to perform these tests
could result in inquiry to, or death of, someone in your care. Staff are to test your Arial® system
regularly. Test all devices at least monthly as described in the product instructions/documentation for each
installed device and be sure that alert and notification signals are received at all Arial PCs and at any other
devices your facility uses to communicate alerts, such as pagers, signs, and smart-phones. Additionally,
you should test your system after power outages, programming changes or upgrades, or after reconfiguring
any system equipment. Failure to regularly test your Arial system could cause you to be unaware of a
system failure. Do not ignore low battery alerts on your devices and replace batteries immediately. Failure
to
replace batteries could result in a call not reaching the Arial system. The Arial system should only be
operated by properly trained personnel.
This deficiency represents non-compliance investigated under Master Complaint OH00150540.
FORM CMS-2567 (02/99)
Previous Versions Obsolete
Event ID:
Facility ID:
365911
If continuation sheet
Page 3 of 3