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Zimmer Biomet, Inc. recalls Affixus Hip Fracture Nail 130 11 mm x 180 mm, Item Number 814511180 Product Usage: Intended for the fixation of frac
Recalled October 24, 2018 · FDA recall Z-0158-2019 · Zimmer Biomet
Hazard
There were complaints indicating that when the product was opened in surgery, the sterile packaging was already open. · FDA Class II
Units
85
Sold at
Worldwide Distribution - US Nationwide in the states of: AK, AL, AR, AZ, CA, CO, FL, GA, HI, IA, ID, IL, IN, KS, KY, LA, MA, MD, ME, MI, MN, MO, MT, NC, NH, NJ, NM, NV, NY, OH, OK, OR, PA, SC, TN, TX, UT, VA, WA, WI, and WY. The products were distributed to the following foreign countries: Chile, Netherlands.
Description
There were complaints indicating that when the product was opened in surgery, the sterile packaging was already open.
Product
Affixus Hip Fracture Nail 130 11 mm x 180 mm, Item Number 814511180 Product Usage: Intended for the fixation of fractures
Manufacturer(s)
Zimmer Biomet, Inc.
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →