Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Vanguard XP Knee System Porous Femoral Component various sizes and Recalled by Biomet, Inc. Due to The anterior/posterior (AP) dimension may be oversized by...
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 XP Knee System Porous Femoral Component various sizes and orientation a total knee replacement system. prosthesis, knee, patella/femorotibial, semi-constrained, uncemented, porous, coated, polymer/metal/polymer
Quantity: 890
Why Was This Recalled?
The anterior/posterior (AP) dimension may be oversized by 0.016 . If the femoral component does not fit as tightly as intended, bony ingrowth may not occur causing loosening of the femoral component. A revision surgery may be necessary.
Where Was This Sold?
This product was distributed to 1 state: UT
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