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Arthrex, Inc. recalls BioSync Anatomic Cotton Wedge, 20 x 4.5 mm.; Used for internal bone fixation for bone fractures, fusions or osteotomies
Recalled June 22, 2016 · FDA recall Z-1961-2016 · Arthrex
Hazard
Potential for polystyrene particulate presence. · FDA Class II
Units
138 total products
Sold at
Distributed in the states of CA, CO, FL, GA, IL, IN, KS, MD, NC, NY, PA, SC, VA, WA, and WI.
Description
Potential for polystyrene particulate presence.
Product
BioSync Anatomic Cotton Wedge, 20 x 4.5 mm.; Used for internal bone fixation for bone fractures, fusions or osteotomies in the ankle and foot.
Manufacturer(s)
Arthrex, Inc.
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →