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, policy review and staff interview the facility failed to ensure
supplemental oxygen delivery devices were changed weekly and stored properly. This affected three
residents (Residents #12, #24 and #28) of three residents reviewed for supplemental oxygen use. The
facility identified 10 residents currently utilizing supplemental oxygen (Residents #4, #11, #12, #14, #22,
#24, #28, #30, #34 and #37).
Residents Affected - Few
Findings include:
1. Review of Resident #12's medical record revealed an admission date of [DATE] with diagnoses that
included pneumonia, congestive heart failure and hypertension.
Physician's orders on [DATE] indicated the use of supplemental oxygen at two liters per minute (lpm) per
nasal canula by oxygen concentrator. Additional orders indicated to change nasal canula every night shift
on Sunday. An additional order on [DATE] identified the use of DuoNeb (aerosolized medication for
shortness of breath) 0.5-2.5 milligrams (mg) per milliliter (ml) via nebulizer every six hours as needed for
shortness of breath from [DATE] for five days until [DATE].
Review of the Treatment Administration Record (TAR) revealed the oxygen tubing and nasal canula
documented as changed on [DATE] and [DATE].
Observation on [DATE] at 10:05 A.M. revealed Resident #12 sitting in a wheelchair in her room. An oxygen
concentrator was observed with the oxygen tubing and nasal canula draped on the oxygen concentrator
without being stored in a protective plastic storage bag. Additional observation revealed a medication
nebulizer lying on the night stand without being in a protective plastic storage bag. The nasal canula,
oxygen tubing, and nebulizer and tubing was dated [DATE].
2. Review of Resident #24's medical record revealed an admission date of [DATE] with diagnoses that
included chronic obstructive pulmonary disease, diabetes mellitus and vascular dementia.
Physician's orders on [DATE] indicated the use of supplement oxygen at two lpm per nasal canula as
needed for shortness of breath. An additional order on [DATE] indicated the use of DuoNeb 0.5-2.5 mg/ml
via nebulizer every six hours as needed.
Observation on [DATE] at 10:10 A.M. revealed Resident #24 was out of her room. An oxygen concentrator
with oxygen tubing and nasal canula was observed. The nasal canula was draped on top of the
concentrator without being in a protective plastic storage bag. A medication nebulizer was observed sitting
on the night stand without being in a protective plastic storage bag.
(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 2
Event ID:
365291
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
365291
B. Wing
A. Building
(X3) DATE SURVEY
COMPLETED
01/27/2025
NAME OF PROVIDER OR SUPPLIER
STREET ADDRESS, CITY, STATE, ZIP CODE
Hall of Fame Rehabilitation and Nursing Center
2714 13th Street NW
Canton, OH 44708
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
Level of Harm - Minimal harm
or potential for actual harm
Residents Affected - Few
3. Review of Resident #28's medical record revealed an admission date of [DATE] with diagnoses that
included chronic obstructive pulmonary disease, congestive heart failure and dependence on supplemental
oxygen.
Physician's orders on [DATE] indicated the use of DuoNeb 0.5-2.5 mg/ml via nebulizer every two hours as
needed for shortness of breath.
Observation on [DATE] at 10:00 A.M. revealed Resident #28 sitting in bed and utilizing supplement oxygen
via a nasal canula. A medication nebulizer was observed sitting on the night stand without being in a
protective plastic storage bag.
On [DATE] at 10:35 A.M. interview with the Director of Nursing and Assistant Director of Nursing revealed
nursing staff change oxygen tubing and nebulizer equipment weekly on Sunday nights and oxygen delivery
equipment is to be stored in plastic protective bags when not in use. They verified Resident's #12, #24 and
#28's nasal canula and nebulizer were not stored correctly. They further verified Resident #28's nasal
canula was not changed since [DATE] and nebulizer orders expired on [DATE].
Review of the undated facility policy titled Oxygen Administration indicated to change oxygen tubing and
mask/canula weekly and as needed if it becomes soiled or contaminated and to keep delivery devices
covered in a plastic bag when not in use.
This deficiency represents non-compliance investigated under Complaint Number OH00161386.
FORM CMS-2567 (02/99)
Previous Versions Obsolete
Event ID:
Facility ID:
365291
If continuation sheet
Page 2 of 2