Handicare Usa Inc recalls Handicare P600 Series Patient Lift Product Usage: A device used to lift and transport a patient from one place to anoth…

Recall date

November 3, 2017

Source

U.S. Food & Drug Administration (FDA) — enforcement report

Recall number

Z-2753-2018

FDA classification

Class II

Brand / firm

Handicare Usa Inc

Sold / distributed

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,

Why it was recalled

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

Class II means using this product may cause temporary or medically reversible health problems; the chance of serious harm is remote.

What was recalled

Handicare P600 Series Patient Lift Product Usage: A device used to lift and transport a patient from one place to another.