Vanguard XP Tibial Tray 71 mm Item # 195249
Class I - DangerousWhat Should You Do?
- Check if you have this product: Lot Number 584220 590500 590510 663160 663180 663170 660420 117730 332670 833200 373020 373040 373030 515030 515020 515040 752090 752070 752080 919240 919230 846510 764370 764380 837780 754480 837770 861200 881500 881510 984430 984400 039230 052240 039240 881530 984390 039220 984420 052260 984410 090340 570960
- 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 locking bar not fully engaging
- Classification:
- Class I - Dangerous
Dangerous or defective products that predictably could cause serious health problems or death.
- Status:
- terminated
Product Information
Full Description:
Vanguard XP Tibial Tray 71 mm Item # 195249
Product Codes/Lot Numbers:
Lot Number 584220 590500 590510 663160 663180 663170 660420 117730 332670 833200 373020 373040 373030 515030 515020 515040 752090 752070 752080 919240 919230 846510 764370 764380 837780 754480 837770 861200 881500 881510 984430 984400 039230 052240 039240 881530 984390 039220 984420 052260 984410 090340 570960
Distribution:
Nationwide distribution
Official Source
Always verify recall information with the official FDA source:
View on FDA.govFDA Recall Number: Z-2532-2019
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