Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Oxford Partial Knee System Left Medial Tibial Trial Tray Size Recalled by Biomet U.K., Ltd. Due to Zimmer Biomet is conducting a medical device field...
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 Biomet U.K., Ltd. directly.
Affected Products
Oxford Partial Knee System Left Medial Tibial Trial Tray Size D Product Usage: Instruments for use with the Oxford Uni Partial Knee System
Quantity: 72 units in total
Why Was This Recalled?
Zimmer Biomet is conducting a medical device field action for various lot-specific Oxford Knee instruments due to potential alumina inclusions in the raw material batch used to produce the affected products. Inclusions contained within the finished product could lead to the cracking and separation of the instrument.
Where Was This Sold?
This product was distributed to 14 states: AR, CA, KS, KY, LA, MA, MO, MT, NJ, NY, NC, OK, SC, TX
About Biomet U.K., Ltd.
Biomet U.K., Ltd. has 26 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report