Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
REF 32-422760 Oxford Uni Knee System Recalled by Biomet U.K., Ltd. Due to Investigation of complaints found excessive use of 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 Biomet U.K., Ltd. directly.
Affected Products
REF 32-422760 Oxford Uni Knee System,Toffee Hammer, non-sterile, found in REF 32-422763 Oxford Mlcroplasty Knee System Tibial instrument Tray small surgical hammer supplied with the Oxford Partial Knee Microplasty Instrument set, used for impacting implants.
Quantity: 430
Why Was This Recalled?
Investigation of complaints found excessive use of the instrument could result in cracking on the weld between the head and the handle, which could lead to part of the head becoming detached from the handle.
Where Was This Sold?
This product was distributed nationwide across all 50 states.
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