Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Dual Mobility Vivacit-E Bearing Recalled by Zimmer Biomet, Inc. Due to The outer package is labeled as a Size...
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
Dual Mobility Vivacit-E Bearing, Model Number 110031009
Quantity: 31
Why Was This Recalled?
The outer package is labeled as a Size C 38 mm, however, the implant inside the package is a Size E 42 mm.
Where Was This Sold?
This product was distributed to 20 states: FL, ID, IL, IN, KY, MD, MA, MI, MN, NJ, NC, OH, OR, PA, SC, TX, UT, VA, WV, 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