Product Wiki · Recalls · U.S. FDA — Device Enforcement

Recall Z-0778-2013 — PREMIER CARE RECLINER 5570/5574 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.

U.S. FDA — Device Enforcement · United States · 2012-09-24 · Class II

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Agency
U.S. FDA — Device Enforcement
Recall identifier
Z-0778-2013
Date of alert
2012-09-24
Country / jurisdiction
United States
Risk level
Class II
Risk type
recall
Brand
Winco Mfg., LLC
Product category
device
Product type
Devices
Barcode (EAN/GTIN)
557100004
Reported risk: 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.
Primary source: https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts

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