Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Vanguard 360 Revision Knee System 75x 5mm Universal Tibial Block Augment Recalled by Zimmer Biomet, Inc. Due to The implant only has one bolt in the...
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 360 Revision Knee System 75x 5mm Universal Tibial Block Augment, Model Number 185224 Intended for use in Total Knee Arthroplasty
Quantity: 16
Why Was This Recalled?
The implant only has one bolt in the sterile package but it should have had two.
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