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

SwiftHook sold as the following: a. Individually as SwiftHook b. Included with Vega505EE mobile lifts Product Usage: The mobile lifts are intended to assist people with functional impairments in scenarios involving physical positioning. — recall Z-0096-2021

U.S. FDA — Device Enforcement · Sweden · 2020-08-21 · Class II

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Agency
U.S. FDA — Device Enforcement
Recall identifier
Z-0096-2021
Date of alert
2020-08-21
Country / jurisdiction
Sweden
Risk level
Class II
Risk type
recall
Brand
Handicare AB
Product category
device
Product type
Devices
Barcode (EAN/GTIN)
70200008
Reported risk: Carry bar may detach during use of mobile lifts and ceiling lifts equipped with the Swifthook component.
Primary source: https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?start_search=1&

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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