Handicare Usa Inc recalls Handicare C Series Patient Lift Product Usage: A device
Recalled Product
Handicare C Series Patient Lift Product Usage: A device used to lift and transport a patient from one place to another.
Hazard / Issue
Premature strap wear and breakage at maximum weight conditions (625 lbs.).
Issued by
FDA
Distribution: Nationwide (United States)
Lot/Code Info: Device Model; 323100, 323102, 323117, 323118, 323120, 323137, 323149, 323150, 323215, 323225, 323237, 323240, 323400, 323417, 323450, 323600, 323602, 323700, 323750, 323840, 323851, 323917, 323117V, and 323150V
View official government recall
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