Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Vanguard 360 Revision System Posterior Augment With Bolt - Product Recalled by Biomet, Inc. Due to Incorrect bolt -tibial bolts in package instead of...
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 360 Revision System Posterior Augment With Bolt - Product Usage: intended for use in knee arthroplasty Item Number: 185422
Quantity: 21 units
Why Was This Recalled?
Incorrect bolt -tibial bolts in package instead of femoral bolts may delay procedure
Where Was This Sold?
This product was distributed nationwide across all 50 states.
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