Home / Recalls / Winco Mfg., LLC / Z-0032-2013

Z-0032-2013 Class II Terminated

Recalled by Winco Mfg., LLC — Ocala, FL

FDA device recall Z-0032-2013 was initiated by Winco Mfg., LLC on Jul 10, 2012 and is designated Class II. 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. The recall status is terminated (terminated May 23, 2013). Affected quantity: 20 chairs.

Recall Details

Product Type: Devices
Report Date: Oct 17, 2012
Initiation Date: Jul 10, 2012
Termination Date: May 23, 2013
Voluntary/Mandated: Voluntary: Firm initiated
Product Quantity: 20 chairs

Product Description

Caremor Cliner is labeled in part: "***Manufactured By Winco***Ocala, FL 34474 www.wincomfg.com***Model No. 535 Serial No. 535A-104522***" 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

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.

Distribution Pattern

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

Code Information

Model Number 5351

Source

Dataset: openFDA device recall enforcement reports
FDA record: This recall in openFDA (JSON)
Enforcement Report: Search FDA's Enforcement Report for Z-0032-2013
openFDA file date: Oct 26, 2026
Loaded by RegDataLab: Oct 27, 2026

These dates say when openFDA published the data file and when RegDataLab last loaded it.

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