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

Recall Z-0303-2017 — ReTurn 7500/7500 Aid, transfer

U.S. FDA — Device Enforcement · United States · 2014-04-15 · Class II

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Agency
U.S. FDA — Device Enforcement
Recall identifier
Z-0303-2017
Date of alert
2014-04-15
Country / jurisdiction
United States
Risk level
Class II
Risk type
recall
Brand
Handicare USA, Inc.
Product category
device
Product type
Devices
Reported risk: During the period of April 2009  May 2011, Handicare AB used a wing handle in which the screw and handle, after repeated tightening, may slide apart. This causes a small amount of play in the attachment of the ladder, which in turn results in high load at the attachment holes of the ladder. Eventually, this may cause mechanical fatigue in the material of the ladder.
Primary source: https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts

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