Designer Care Cliner 6700/6704/6710 WITH CAL TB 133 UPGRADE PURCHASED JAN 01, 2011 TO AUGUST 20, 2012. A multi position recliner with a steel frame used primarily in clinics, hospitals, and treatment centers for recovery, dialysis, oncology, examination, infusion.
FDA Recall Z-0780-2013 · Posted 2013-02-04
Recalling FirmWinco Mfg., LLC
Recall StatusTerminated
Product CodeINM
Date Initiated2012-09-24
Date Terminated2013-05-23
Product Quantity95 units (All models)
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.
Firm Action
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 [email protected].
For questions regarding this recall call 352-854-2929, ext 110.
Root Cause
Component design/selection
Distribution Pattern
Nationwide Distribution including CA, FL, IL, MA, MD, MN, NM, NY, OH, OK, and TX.
Official Source
View FDA Recall →Source: FDA Enforcement Report / Recall database. Always confirm against the official FDA record.