Atlas FDA

NOCTURNAL ELITE CARE CLINER 6980(STD)/6990(X-LG) products are labeled in part: "***NOCTURNAL ELITE CARE CLINER 6980/6990

FDA device recall Z-1461-2012 · posted 2012-04-25 · Terminated

Recall details

Recalling firm
Winco Mfg., LLC
Reason for recall
Winco Manufacturing LLC is recalling the Care Cliner, XL Care Cliner, Drop Arm Care Cliner, Elite Care Cliner, and XL Elite Care Cliner chairs with nylon casters distributed between 04/01/2009 and 08/31/2009. Certain 5" nylon casters shipped with the chairs may be defective. There is a potential of the caster's axle working itself out of the assembly under unconventional conditions. Should this
Action taken
Winco Mfg. sent an "URGENT DEVICE RECALL" letter dated February 1, 2012 to all affected customers. The letter identifies the product, problem, and actions to be taken by the customers. Customers were asked to complete the Caster Recall Replacement Form and return it to the firm's Customer Service Department via fax to 352-854-9544. Contact the Customer Service Department at 800 237-3377 for questions regarding this notice.
Root cause
Device Design
Status
Terminated
Product code
INM
Quantity affected
96 Casters (32 Chairs)
Distribution
Worldwide Distribution-USA (nationwide) and the countries of Canada and Singapore.
Date initiated
2012-02-06
Date posted
2012-04-25
Date terminated
2012-07-27
Location
Ocala, FL

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