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

Recall Z-1613-2015 — ReTurn belt, wipeable, sizes Small through Extra Large, Plastic pouch, 1 item per pouch. Patient transfer aid.

U.S. FDA — Device Enforcement · United States · 2015-03-26 · Class II

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Agency
U.S. FDA — Device Enforcement
Recall identifier
Z-1613-2015
Date of alert
2015-03-26
Country / jurisdiction
United States
Risk level
Class II
Risk type
recall
Brand
Handicare USA, Inc.
Product category
device
Product type
Devices
Reported risk: Complaints were received that the heat-welded seam on the wipeable belt's strap tore when force was applied.
Primary source: https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts

Verify each fact at the issuing agency before acting. Recall scope, affected lots, and remediation instructions may be updated by the agency after our last sync.

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