Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
(1) Vanguard Knee System PS Open Box Femoral Recalled by Biomet, Inc. Due to Components Incorrectly labeled as either smaller or larger...
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
(1) Vanguard Knee System PS Open Box Femoral; Right; 60 mm. Intended for knee joint replacement prostheses. Item Number: 183104 (2) Vanguard Knee System PS Open Box Femoral; Right; 62.5 mm Item Number: 183106 (3) Vanguard Knee System PS Open Box Femoral; Right; 65 mm Item Number: 183108 (4) Vanguard Knee System PS Open Box Femoral; Right; 67.5 mm Item Number: 183110 (5) Vanguard Knee System PS Open Box Femoral; Right; 70 mm Item Number: 183112
Quantity: 157 units
Why Was This Recalled?
Components Incorrectly labeled as either smaller or larger and incorrect side (right/left).
Where Was This Sold?
This product was distributed to 6 states: FL, IN, MD, OH, PA, WI
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