Compress Device Short Anchor Plug, 14 MM-For Correction of revision of unsuccessful osteotomy, arthrodesis, or previous joint replacement. Item Number: 178556
Class I - DangerousWhat Should You Do?
- Check if you have this product: Lot Numbers/UDI: 331710 (01)00880304461635(17)270702(10)331710; 331720 (01)00880304461635(17)270723(10)331720; 331730 (01)00880304461635(17)270629(10)331730; 331740 (01)00880304461635(17)270726(10)331740; 477990 (01)00880304461635(17)270820(10)477990; 541450 (01)00880304461635(17)270725(10)541450; 577360 (01)00880304461635(17)270801(10)577360; 577690 (01)00880304461635(17)270814(10)577690; 577700 (01)00880304461635(17)270725(10)577700; 608540 (01)00880304461635(17)270902(10)608540; 608650 (01)00880304461635(17)271030(10)608650; 608670 (01)00880304461635(17)271030(10)608670; 671830 (01)00880304461635(17)270901(10)671830; 829350 (01)00880304461635(17)270823(10)829350
- 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 Short Anchor Plug, 14 MM-For Correction of revision of unsuccessful osteotomy, arthrodesis, or previous joint replacement. Item Number: 178556
Product Codes/Lot Numbers:
Lot Numbers/UDI: 331710 (01)00880304461635(17)270702(10)331710; 331720 (01)00880304461635(17)270723(10)331720; 331730 (01)00880304461635(17)270629(10)331730; 331740 (01)00880304461635(17)270726(10)331740; 477990 (01)00880304461635(17)270820(10)477990; 541450 (01)00880304461635(17)270725(10)541450; 577360 (01)00880304461635(17)270801(10)577360; 577690 (01)00880304461635(17)270814(10)577690; 577700 (01)00880304461635(17)270725(10)577700; 608540 (01)00880304461635(17)270902(10)608540; 608650 (01)00880304461635(17)271030(10)608650; 608670 (01)00880304461635(17)271030(10)608670; 671830 (01)00880304461635(17)270901(10)671830; 829350 (01)00880304461635(17)270823(10)829350
Official Source
Always verify recall information with the official FDA source:
View on FDA.govFDA Recall Number: Z-0380-2024
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