Medical device recalls Moderate risk

Getinge Dominican Republic SA recalls Arjo Disposable Repositioning Sling, Model AHD001

Recall date
July 30, 2021
Source
U.S. Food & Drug Administration (FDA) — enforcement report
Recall number
Z-2470-2021
FDA classification
Class II
Brand / firm
Getinge Dominican Republic SA
Sold / distributed
US Nationwide distribution in the states of AL, AR, AZ, CA, CO, CT, FL, GA, IA, IL, IN, KS, KY, MD, ME, MI, MN, MO, MS, NC, ND, NJ, NM, NY, OH, OR, PA, SC, TN, TX, VA, VT, WI, and WV.

Why it was recalled

Sling loop straps on device pose a trip hazard.

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

What was recalled

Arjo Disposable Repositioning Sling, Model AHD001

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