FDAApril 15, 2014device
ReTurn 7500/7500 Aid, transfer
Official recall recorded by the U.S. Food & Drug Administration.
The hazard
During the period of April 2009 May 2011, Handicare AB used a wing handle in which the screw and handle, after repeated tightening, may slide apart. This causes a small amount of play in the attachment of the ladder, which in turn results in high load at the attachment holes of the ladder. Eventually, this may cause mechanical fatigue in the material of the ladder.
What to do
FDA enforcement status: Terminated
Brands named
handicare
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
- 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
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