Compress Device Segmental Anchor Plug, 24 MM-For Correction of revision of unsuccessful osteotomy, arthrodesis, or previous joint replacement. Item Number: 178414
Class I - DangerousWhat Should You Do?
- Check if you have this product: Lot Numbers/UDI 017930 (01)00880304259829(17)270702(10)017930; 018070 (01)00880304259829(17)270629(10)018070; 608560 (01)00880304259829(17)271030(10)608560 752820 (01)00880304259829(17)280222(10)752820 752830 (01)00880304259829(17)270817(10)752830
- 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:
- Anchor plugs potentially have metal burrs in the transverse holes of the device, preventing the drill or pins from passing through, may result in extension of surgery
- Classification:
- Class I - Dangerous
Dangerous or defective products that predictably could cause serious health problems or death.
- Status:
- ongoing
Product Information
Full Description:
Compress Device Segmental Anchor Plug, 24 MM-For Correction of revision of unsuccessful osteotomy, arthrodesis, or previous joint replacement. Item Number: 178414
Product Codes/Lot Numbers:
Lot Numbers/UDI 017930 (01)00880304259829(17)270702(10)017930; 018070 (01)00880304259829(17)270629(10)018070; 608560 (01)00880304259829(17)271030(10)608560 752820 (01)00880304259829(17)280222(10)752820 752830 (01)00880304259829(17)270817(10)752830
Official Source
Always verify recall information with the official FDA source:
View on FDA.govFDA Recall Number: Z-0377-2024
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