Atlas FDA

Caremor Cliner"***Manufactured By Winco***Ocala, FL 34474 www.wincomfg.com***Model No. 536 Serial No. 536A-101475***" Li

FDA device recall Z-0031-2013 · posted 2012-10-10 · Terminated

Recall details

Recalling firm
Winco Mfg., LLC
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.
Action taken
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.
Root cause
Process control
Status
Terminated
Product code
INM
Quantity affected
23 chairs
Distribution
Worldwide Distribution - USA including Arkansas, California, Maryland, Mississippi, New York, Pennsylvania and the country of Saudi Arabia
Date initiated
2012-07-10
Date posted
2012-10-10
Date terminated
2013-05-23
Location
Ocala, FL

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