CLASS II Device recall · Reported 5 Mar 2014 · FDA Enforcement Report

XL Convalescent Recliner 5291/529S with Padded armrests recalled

Winco Mfg is recalling XL Convalescent Recliner 5291/529S with Padded armrests with guard, Dual fold down, distributed nationwide in the US. The recall was initiated on 6 Sep 2013 and the FDA has classified it as Class II.

Check your package

Lot, batch or date codesModel(s) 5291, 529S. Serial numbers: 529A003767, 529A003779, 529A003787, 529A003790, 529A003792 thru 529A003865, 529S100044 thru 529100050.

Quantity recalled369 units (all models)

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-1117-2014
FDA event ID: 67377
Recalling firm: Winco Mfg, Ocala, FL
Classification: Class II
Status: Terminated
Recall initiated: 6 Sep 2013
FDA classified: 26 Feb 2014
Reported: 5 Mar 2014
Type: Voluntary: Firm initiated
Customers notified by: Letter
Reason category: Device Malfunction
Device type: Other Medical Devices

Timeline

6 Sep 2013	Recall initiated by company
26 Feb 2014	Classified by FDA	+173 days
5 Mar 2014	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

A supplier manufacturing assembly defect with the right hand recline mechanism. Use of this product may result in the loss of functionality of the three (3) position lock bar when in a reclined position.

Device recalls are issued when a component, software or design fault could cause the device to fail or give wrong readings. Many are corrections applied in the field rather than physical returns.

Product as listed by the FDA

XL CONVALESCENT RECLINER 5291/529S with Padded armrests with guard, Dual fold down side-tables, Removable side panels, Built-in head-rest. The products are a multi position recliners with a steel frame used primarily in long term care or convalescent facilities. The recliners are suitable as general purpose seating for relaxation, reclining, eating, patient transport within the facility, and as a patient room chair for visitors.

Where it was distributed

Worldwide Distribution - USA nationwide including Alabama, Arkansas, Arizona, California, Colorado, Connecticut, Florida, Georgia, Idaho, Illinois, Indiana, Kanas, Kentucky, Louisiana, Massachusetts, Maryland, Maine, Michigan, Minnesota, Missouri, Mississippi, North Carolina, North Dakota, New Jersey, New Mexico, New York, Ohio, Oklahoma, Pennsylvania, South Carolina, South Dakota, Tennessee, Texas, Virginia, Vermont, Washington, Wisconsin, West Virginia, Puerto Rico and Internationally to the country of Canada.

Nationwide Alabama Arkansas Arizona California Colorado Connecticut Florida Georgia Idaho Illinois Indiana Kentucky Louisiana Massachusetts Maryland Maine Michigan Minnesota Missouri Mississippi

Stores named: WinCo

Questions about this recall

Why was it recalled?

Which lots are affected?

Model(s) 5291, 529S. Serial numbers: 529A003767, 529A003779, 529A003787, 529A003790, 529A003792 thru 529A003865, 529S100044 thru 529100050.

Where was it sold?

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

3 other products · FDA event 67377

This product is part of a recall event; the main page for the event is Premier Care Recliner 5570 with Urethane armrests recalled by Winco Mfg.

Reported	Class	Recall	Company	Reason	Where
5 Mar 2014	CLASS II	Premier Care Recliner 5570 with Urethane armrests recalled by Winco Mfg	Winco Mfg	Device Malfunction	Nationwide
5 Mar 2014	CLASS II	Convalescent Recliner 5251/5261, 525S/526S recalled by Winco Mfg	Winco Mfg	Device Malfunction	Nationwide
5 Mar 2014	CLASS II	Drop-arm Convalescent Recliner 5271/5281 recalled by Winco Mfg	Winco Mfg	Device Malfunction	Nationwide

More recalls from Winco Mfg

All 26

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19 Oct 2016Device	CLASS II	TransMotion Medical, TMM4 Series Multi-Purpose Treatment Chair recalled	Winco Mfg	Other	29 states
19 Oct 2016Device	CLASS II	TransMotion Medical, TMM3 Series Video-Fluoroscopy Swallow recalled	Winco Mfg	Other	29 states
26 Aug 2015Device	CLASS II	Winco Designer Care Cliner - with Nylon Casters Oncology recalled	Winco Mfg	Other	Nationwide
26 Aug 2015Device	CLASS II	Winco Elite Care Cliner w/Swing Away Arms X-Large recalled by Winco Mfg	Winco Mfg	Other	Nationwide

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