Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Vanguard Complete Knee System Recalled by Zimmer Biomet, Inc. Due to Knee implant components (tibial bearings) are labeled with...
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 Zimmer Biomet, Inc. directly.
Affected Products
Vanguard Complete Knee System, Vanguard CR Lipped Tibial Bearing 10x71/75, Item Number: 183540 Product Usage: For use in total knee arthroplasty
Quantity: 24
Why Was This Recalled?
Knee implant components (tibial bearings) are labeled with the incorrect size.
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About Zimmer Biomet, Inc.
Zimmer Biomet, Inc. has 875 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report