Medical DeviceOct 21, 2020
Handicare AB SwiftHook sold as the following: a recall — FDA Z-0096-2021
Carry bar may detach during use of mobile lifts and ceiling lifts equipped with the Swifthook component.
Class IIFDA: TerminatedHandicare AB
Recall history in this database
Classification mix: Class II: 1.
Understanding this recall history
This page summarizes recall records in which the official source identifies Handicare AB as the recalling firm or manufacturer. The number of records should not be treated as a safety rating or a measure of company size, because recall counts depend on product mix, reporting periods and how government records are organized.
Compare the dates, categories and classifications together rather than relying on the total alone. Open an individual record for the recalled product, reason, distribution details and current instructions available from the source.