Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Vanguard M Unicondylar Tibial Trial For use during knee joint replacement. Recalled by Biomet, Inc. Due to The Left and Right orientation of the trial...
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, Inc. directly.
Affected Products
Vanguard M Unicondylar Tibial Trial For use during knee joint replacement.
Quantity: 27
Why Was This Recalled?
The Left and Right orientation of the trial was incorrectly etched on one side. When the instrument is rotated about the axis of the handle 180 degrees to view the other side, the etch on the handle now shows R on the same side as the keel marked LM and the L on the same side as the keel marked RM. This is incorrect. Please note that the keel is not etched on this side by design.
Where Was This Sold?
This product was distributed to 2 states: IL, NJ
About Biomet, Inc.
Biomet, Inc. has 250 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report