A.L.P.S. - Medium Bone Plate Forceps. Orthopedic manual surgical instrument.
Class I - DangerousWhat Should You Do?
- Check if you have this product: Part Number: 816301006 Lot Numbers: 099216, 093776, 093717, 093716, 088526, 081179, 072525, 072524
- 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:
- Biomet, Inc.
- Reason for Recall:
- Medium Bone Plate Forceps was assembled with the incorrect grip arm tip. Potential that the surgeon will be unable to provisionally clamp the plate to the patient's bone.
- Classification:
- Class I - Dangerous
Dangerous or defective products that predictably could cause serious health problems or death.
- Status:
- terminated
Product Information
Full Description:
A.L.P.S. - Medium Bone Plate Forceps. Orthopedic manual surgical instrument.
Product Codes/Lot Numbers:
Part Number: 816301006 Lot Numbers: 099216, 093776, 093717, 093716, 088526, 081179, 072525, 072524
Distribution:
Distributed in: TX, NJ, NC, KY, MA, SD, MO, AL, IN, GA, AR
Official Source
Always verify recall information with the official FDA source:
View on FDA.govFDA Recall Number: Z-2072-2015
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