Atlas FDA

Designer Care Cliner 6700/6704/6710 WITH CAL TB 133 UPGRADE PURCHASED JAN 01, 2011 TO AUGUST 20, 2012. A multi position

FDA device recall Z-0780-2013 · posted 2013-02-04 · Terminated

Recall details

Recalling firm
Winco Mfg., LLC
Reason for recall
The performance of the chemicals in the foam and vinyl are not consistent enough to meet the TB 133 fire protection mandate required by California and 4 other states.
Action taken
Winco sent a Chair Field Correction Notification dated September 24, 2012, to all affected consignees. The letter identified the product, the problem, and the action to be taken by the consignee. The consignees were instructed to forward the "Field Correction Form - REPAIR" form back to Winco and the firm would send a Winco Representative to the consignees' facility to correct the chairs in the field. Customers with questions were instructed to contact Winco at 800-237-3377 or email customerservice@wincomfg.com. For questions regarding this recall call 352-854-2929, ext 110.
Root cause
Component design/selection
Status
Terminated
Product code
INM
Quantity affected
95 units (All models)
Distribution
Nationwide Distribution including CA, FL, IL, MA, MD, MN, NM, NY, OH, OK, and TX.
Date initiated
2012-09-24
Date posted
2013-02-04
Date terminated
2013-05-23
Location
Ocala, FL

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