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Handicare Usa Inc recalls Handicare P600 Series Patient Lift Product Usage: A device used to lift and transport a patient from one place to anot
Recalled August 29, 2018 · FDA recall Z-2753-2018 · Handicare Usa
Hazard
Premature strap wear and breakage at maximum weight conditions (625 lbs.). · FDA Class II
Units
4
Sold at
Worldwide Distribution - US Nationwide in the states of AK, CA, CT, DE, GA, IA, IL, KY, LA, MA, ME, MI, MN, MO, NE, NV, NY, OH, OR, PA, RI, TN, TX, WI, and Puerto Rico and the countries of Canada and Australia,
Description
Premature strap wear and breakage at maximum weight conditions (625 lbs.).
Product
Handicare P600 Series Patient Lift Product Usage: A device used to lift and transport a patient from one place to another.
Manufacturer(s)
Handicare Usa Inc
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →