Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Vanguard Knee System -PS Open Box Femoral Right Recalled by Zimmer Biomet, Inc. Due to Label on the outer carton or the patient...
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 Knee System -PS Open Box Femoral Right, 65 mm Item Number:183108
Quantity: 8 units
Why Was This Recalled?
Label on the outer carton or the patient labels does not match label on the inner sterile packaging
Where Was This Sold?
This product was distributed to 7 states: AR, MN, MO, NJ, NY, OH, VA
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