CLASS II Device recall · Reported 27 Oct 2021 · FDA Enforcement Report

Easi-Care Gait Belt Metal Buckle (54", 60", and 72" lengths) recalled

Kinsman Enterprises is recalling Easi-Care Gait Belt Metal Buckle (54", 60", and 72" lengths), distributed in 14 states. The recall was initiated on 10 Sep 2021 and the FDA has classified it as Class II.

Check your package

Lot, batch or date codesKinsman Product Numbers: 80805 (54"), 80806 (60"), and 80807 (72") UPC codes: 873704007275, 873704006773, 873704007282

Quantity recalled13,123 units

Stop using the device if the notice says to, and contact the manufacturer or your healthcare provider for the correction or replacement.

Recall details

Recall number: Z-0161-2022
FDA event ID: 88760
Recalling firm: Kinsman Enterprises, W Frankfort, IL
Classification: Class II
Status: Terminated
Recall initiated: 10 Sep 2021
FDA classified: 21 Oct 2021
Reported: 27 Oct 2021
Type: Voluntary: Firm initiated
Customers notified by: E-Mail
Reason category: Foreign Material
Device type: Other Medical Devices

Timeline

10 Sep 2021	Recall initiated by company
21 Oct 2021	Classified by FDA	+41 days
27 Oct 2021	Published in enforcement report	+6 days

Companies usually start a recall weeks before the FDA classifies and publishes it; the gap above is that lag.

Reason for recall

The belt may fail at lower loads than the labeled 600lbs.

Foreign material recalls cover pieces of metal, plastic, glass, wood or other objects that got into the product during processing and could cause injury if eaten.

Product as listed by the FDA

Easi-Care Gait Belt Metal Buckle (54", 60", and 72" lengths)

Where it was distributed

Distribution in CA, FL, GA, IL, KY, MI, MS, NC, NH, NJ, NY, OH, TN, VA

California Florida Georgia Illinois Kentucky Michigan Mississippi North Carolina New Hampshire New Jersey New York Ohio Tennessee Virginia

Questions about this recall

Why was it recalled?

The belt may fail at lower loads than the labeled 600lbs.

Which lots are affected?

Kinsman Product Numbers: 80805 (54"), 80806 (60"), and 80807 (72") UPC codes: 873704007275, 873704006773, 873704007282

Where was it sold?

Distribution in CA, FL, GA, IL, KY, MI, MS, NC, NH, NJ, NY, OH, TN, VA

What should I do if I have it?

Stop using the device if the notice says to, and contact the manufacturer or your healthcare provider for the correction or replacement.

What does Class II mean?

Class II means the product may cause temporary or medically reversible health problems, or the probability of serious harm is remote.

Read the official FDA notice · Source record retrieved 26 Sep 2026. The FDA describes openFDA data as unvalidated; the official notice takes precedence. This page reports the record and gives no medical advice.

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