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

A-series lift - A625 Manual Part No. 324117. Prism Medical. — recall Z-1406-2017

U.S. FDA — Device Enforcement · United States · 2017-01-30 · Class II

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Agency
U.S. FDA — Device Enforcement
Recall identifier
Z-1406-2017
Date of alert
2017-01-30
Country / jurisdiction
United States
Risk level
Class II
Risk type
recall
Brand
ErgoSafe Products, LLC (DBA) Prism Medical
Product category
device
Product type
Devices
Reported risk: During internal cycle test at max load (625 lbs.) 2 units had straps break prematurely.
Primary source: https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?start_search=1&

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