Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Ziptight Ankle Syndesmosis Fixation Device Recalled by Zimmer Biomet, Inc. Due to Ziptight Ankle Syndesmosis Fixation was packaged without the...
What You Should Do
Stop using this product immediately. Do not consume, use, or distribute it.
Return the product to the place of purchase for a full refund. If you have questions, contact Zimmer Biomet, Inc. directly.
Affected Products
Ziptight Ankle Syndesmosis Fixation Device, Titanium Implant Titanium Implant for surgical repairs of soft tissue.
Quantity: 885 units total
Why Was This Recalled?
Ziptight Ankle Syndesmosis Fixation was packaged without the tip protectors.
Where Was This Sold?
This product was distributed to 29 states: AL, AK, AZ, AR, CA, CO, FL, ID, IN, KY, ME, MD, MA, MI, MN, MO, NY, NC, OH, OK, OR, PA, SC, TN, TX, UT, VA, WA, WI
About Zimmer Biomet, Inc.
Zimmer Biomet, Inc. has 875 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report