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Zimmer Biomet, Inc. recalls Ziptight Ankle Syndesmosis Fixation Device, Titanium Implant Titanium Implant for surgical repairs of soft tissue.
Recalled March 7, 2018 · FDA recall Z-0818-2018 · Zimmer Biomet
Hazard
Ziptight Ankle Syndesmosis Fixation was packaged without the tip protectors. · FDA Class II
Units
885 units total
Sold at
Distributed domestically to AK, AL, AR, AZ, CA, CO, FL, ID, IN, KY, MA, MD, ME, MI, MN, MO, NC, NY, OH, OK, OR, PA, SC, TN, TX, UT, VA, WA, WI. Distributed internationally to ARGENTINA, AUSTRALIA, CANADA, COSTA RICA, JAPAN, NETHERLANDS.
Description
Ziptight Ankle Syndesmosis Fixation was packaged without the tip protectors.
Product
Ziptight Ankle Syndesmosis Fixation Device, Titanium Implant Titanium Implant for surgical repairs of soft tissue.
Manufacturer(s)
Zimmer Biomet, Inc.
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →