Recall Z-0031-2013— Winco Mfg., LLC

Class II FDA medical device recall by Winco Mfg., LLC, initiated 2012-07-10, terminated 2013-05-23. FDA's recall record names no specific 510(k) clearance for this event. 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. Reason: 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..

Recalling firm

Winco Mfg., LLC

Classification

Class II

Status

Terminated

Initiated

2012-07-10

Terminated

2013-05-23

Firm location

Ocala, FL, United States

Data sourced from openFDA. This site is unofficial and independent of the FDA.