FDAJune 15, 2016device
EVA Floor Lifts, Model Numbers: 400, 450, 600
Official recall recorded by the U.S. Food & Drug Administration.
The hazard
After feedback from customers and internal suspicion, Handicare has become aware that abnormal use of Eva-lifts could lead to a deterioation in the joint of the liftarm. This could lead to injury if the joint breaks. All lifts must therefore be checked and reported back to the manuafacturer.
What to do
FDA enforcement status: Ongoing
Brands named
handicare abhandicare
Recall history
Other federal recalls tied to the same brand — a factual pattern, straight from the source data.
- FDASwiftHook 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.2020-08-21
- 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
- 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
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