Vanguard CR Porous Femoral 62.5mm (Left Femur) For use in total knee arthroplasty
Class I - DangerousWhat Should You Do?
- Check if you have this product: Item #183066/Lot 132900; UDI-(01) 0088030427068 (17) 270816 (10) 132900
- Do not eat it: Even if it looks and smells fine, do not consume this product.
- Throw it away or return it: You can return the product to the store for a full refund.
- Seek medical attention if needed: If you've consumed this product and feel unwell, contact your doctor immediately.
- Report problems: Report any issues to the FDA's Safety Reporting Portal.
⚠️ Emergency: If you experience severe symptoms after consuming this product, call 911 or Poison Control at 1-800-222-1222.
Recall Details
- Company:
- Zimmer Biomet, Inc.
- Reason for Recall:
- The affected products are labeled as a 62.5mm LEFT Femur; however, the contents are a Vanguard 70mm RIGHT Femur.
- Classification:
- Class I - Dangerous
Dangerous or defective products that predictably could cause serious health problems or death.
- Status:
- terminated
Product Information
Full Description:
Vanguard CR Porous Femoral 62.5mm (Left Femur) For use in total knee arthroplasty
Product Codes/Lot Numbers:
Item #183066/Lot 132900; UDI-(01) 0088030427068 (17) 270816 (10) 132900
Distribution:
Distributed in: US, FL, WI, MD, MO, MI
Official Source
Always verify recall information with the official FDA source:
View on FDA.govFDA Recall Number: Z-1011-2018
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