Z-0031-2013Class II

Caremor Cliner"Manufactured By WincoOcala, FL 34474 www.wincomfg.com***Model No. 536 Serial No...

Name: Z-0031-2013 Caremor Cliner"***Manufactured By Winco***Ocala, FL 34474 www.wincomfg.com***Model No. 536 Serial No...
Creator: Winco Mfg., LLC
Published: 2012-07-10
License: https://open.fda.gov/license/

Champion Mfg, Inc. / initiated 2012-07-10 / Terminated / root cause: manufacturing process

FDA source

Winco Mfg., LLC began a recall of Caremor Cliner"***Manufactured By Winco***Ocala, FL 34474 www.wincomfg.com***Model No. 536 Serial No. 536A-101475***" Literature: "***Caremor Cliner... on 2012-07-10. FDA classified it as Class II and gives the reason as "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". As of 2026-09-10, the recall status on record is Terminated, and MDM tags the root cause as manufacturing process.

Recall record

Recall number: Z-0031-2013
Classification: Class II
Status: Terminated
Initiated: 2012-07-10
Posted: 2012-10-10
Terminated: 2013-05-23
Recalling firm: Champion Mfg, Inc.
Product: 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
Product code: INM Chair, With Casters
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.
Root cause tag: manufacturing process
FDA root cause: Process control
Action: Winco notified consignees via phone except for the one located in Saudi Arabia, who was contacted by e-mail. All consignees have been sent a follow-up e-mail. The notification identified the product, the problem, and the action to be taken to be taken by the customer. Customers should remove the chair from use and the upholstered back will not be required to be returned. Winco will send out new fully assembled upholstered backs. For questions customers should call 352-854-2929, ext 123.
Quantity in commerce: 23 chairs
Distribution: Worldwide Distribution - USA including Arkansas, California, Maryland, Mississippi, New York, Pennsylvania and the country of Saudi Arabia
Product codes and lots: Model Number 5361

Enforcement reports

One row per recalled product line

FDA enforcement reports joined to recall event Z-0031-2013
Recall number	Class	Status	Voluntary or mandated	Report date	Classified
Z-0031-2013	Class II	Terminated	Voluntary: Firm initiated	2012-10-17	2012-10-10
Z-0032-2013	Class II	Terminated	Voluntary: Firm initiated	2012-10-17	2012-10-10

Product code INM

The FDA recall record names no cleared device, and no clearance has been matched to it.

MDM coverage of this record lists here, newest first.

About this record

Sourced from the FDA device recall database and the FDA enforcement reports, both ingested from openFDA. The recall record supplies the product, the reason and the product code; the enforcement report supplies the classification. The two datasets are exported by FDA on different days, and the date above is the older of the two, so nothing on this page is newer than it says.

MDM adds the root cause tag, derived from FDA’s own root cause text, and the cross-links to the product code, the clearances named on the record and MDM coverage. Where a recall has not been joined to an enforcement report, no classification is shown.

Data as of 2026-10-07, the FDA export date for this dataset. Page last changed 2026-09-05. View this recall on fda.gov (opens on fda.gov)