FDAAugust 21, 2020device
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.
Official recall recorded by the U.S. Food & Drug Administration.
The hazard
Carry bar may detach during use of mobile lifts and ceiling lifts equipped with the Swifthook component.
What to do
FDA enforcement status: Terminated
Brands named
handicare abhandicare
UPCs
733176902042266031185404226603118560422
Recall history
Other federal recalls tied to the same brand — a factual pattern, straight from the source data.
- FDAHandicare C Series Patient Lift Product Usage: A device used to lift and transport a patient from one place to another.2017-11-03
- FDAHandicare P600 Series Patient Lift Product Usage: A device used to lift and transport a patient from one place to another.2017-11-03
- FDAPRISM MEDICAL A-625, MAX. LOAD 625 lbs. 283 Kgs., Patient lift, non-A/C powered2017-09-08
- FDACarina Mobile Lifts, Models: a) Carina350EM, REF 6060011 b) Carina350EML, REF 60600012 c) Carina350EE, REF 606000092016-07-28
- FDAEVA Floor Lifts, Model Numbers: 400, 450, 6002016-06-15
- FDAReTurn belt, wipeable, sizes Small through Extra Large, Plastic pouch, 1 item per pouch. Patient transfer aid.2015-03-26
- FDAReTurn 7500/7500 Aid, transfer2014-04-15
Own something like this?
AllClear screens your whole list against every CPSC, FDA, USDA and NHTSA recall — and tells you the day a new one names something you own.
Start free — 200 items, no card →