FDANovember 3, 2017device

Handicare C Series Patient Lift Product Usage: A device used to lift and transport a patient from one place to another.

Official recall recorded by the U.S. Food & Drug Administration.

The hazard

Premature strap wear and breakage at maximum weight conditions (625 lbs.).

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.

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