CLASS II Device recall · Reported 17 Oct 2012 · FDA Enforcement Report

Caremor Cliner"*** recalled by Winco Mfg

Winco Mfg is recalling Caremor Cliner"***, distributed in Arkansas, California, Maryland, Mississippi, New York, Pennsylvania. The recall was initiated on 10 Jul 2012 and the FDA has classified it as Class II.

Check your package

Lot, batch or date codesModel Number 5361

Quantity recalled23 chairs

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-0031-2013
FDA event ID: 63085
Recalling firm: Winco Mfg, Ocala, FL
Classification: Class II
Status: Terminated
Recall initiated: 10 Jul 2012
FDA classified: 10 Oct 2012
Reported: 17 Oct 2012
Type: Voluntary: Firm initiated
Customers notified by: Telephone
Reason category: Other Reasons
Device type: Other Medical Devices

Timeline

10 Jul 2012	Recall initiated by company
10 Oct 2012	Classified by FDA	+92 days
17 Oct 2012	Published in enforcement report	+7 days

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

Reason for recall

Winco Mfg., LLC in Ocala, FL is recalling the Caremor Cliner model numbers 5351 and 5361. The recall was initiated due to a report that a back frame did not "snap" onto a chair frame properly.

Product as listed by the FDA

Caremor Cliner"***Manufactured By Winco***Ocala, FL 34474 www.wincomfg.com***Model No. 536 Serial No. 536A-101475***" Literature: "***Caremor Cliner 5351/5361***Winco***ISO 9001-2008 Certified***Our most comfortable and versatile recliner***Ease of operation, outstanding durability, and exceptional value have made this one of our bestselling recliners. The Caremor Cliner provides patient comfort and support as well as user friendly features.***KEY FEATURE'S***Infinite positioning back***Padded armrests w/arm guard***Webbed elastic suspension back and seat***Removable side panels**Continuous seat & legrest cushion***5351 w/tray***5361 w/out tray***1.800.237.3377***5516 SW 1st Lane***Ocala, Florida 34474***www.wincomfg.com***Proudly Made in the USA***" Patient recliner chair

Where it was distributed

Worldwide Distribution - USA including Arkansas, California, Maryland, Mississippi, New York, Pennsylvania and the country of Saudi Arabia

Arkansas California Maryland Mississippi New York Pennsylvania

Stores named: WinCo

Questions about this recall

Why was it recalled?

Winco Mfg., LLC in Ocala, FL is recalling the Caremor Cliner model numbers 5351 and 5361. The recall was initiated due to a report that a back frame did not "snap" onto a chair frame properly.

Which lots are affected?

Model Number 5361

Where was it sold?

Worldwide Distribution - USA including Arkansas, California, Maryland, Mississippi, New York, Pennsylvania and the country of Saudi Arabia

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.

Other products in this recall event

1 other product · FDA event 63085

Reported	Class	Recall	Company	Reason	Where
17 Oct 2012	CLASS II	Caremor Cliner is labeled in part: "*** recalled by Winco Mfg	Winco Mfg	Other	6 states

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