Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Vanguard CR Porous Femoral 62.5mm (Left Femur) For use in Recalled by Zimmer Biomet, Inc. Due to The affected products are labeled as a 62.5mm...
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 CR Porous Femoral 62.5mm (Left Femur) For use in total knee arthroplasty
Quantity: 8
Why Was This Recalled?
The affected products are labeled as a 62.5mm LEFT Femur; however, the contents are a Vanguard 70mm RIGHT Femur.
Where Was This Sold?
This product was distributed to 5 states: FL, MD, MI, MO, WI
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