Compress Device Short Anchor Plug, 20 MM-For Correction of revision of unsuccessful osteotomy, arthrodesis, or previous joint replacement. Item Number: 178562
Class I - DangerousWhat Should You Do?
- Check if you have this product: Lot Numbers/UDI: 331820 (01)00880304461666(17)270710(10)331820; 478000 (01)00880304461666(17)270629(10)478000; 535420 (01)00880304461666(17)270826(10)535420; 608710 (01)00880304461666(17)271114(10)608710; 608740 (01)00880304461666(17)271113(10)608740; 671500 (01)00880304461666(17)271030(10)671500; 671510 (01)00880304461666(17)280121(10)671510; 857040 (01)00880304461666(17)271112(10)857040;
- 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, 20 MM-For Correction of revision of unsuccessful osteotomy, arthrodesis, or previous joint replacement. Item Number: 178562
Product Codes/Lot Numbers:
Lot Numbers/UDI: 331820 (01)00880304461666(17)270710(10)331820; 478000 (01)00880304461666(17)270629(10)478000; 535420 (01)00880304461666(17)270826(10)535420; 608710 (01)00880304461666(17)271114(10)608710; 608740 (01)00880304461666(17)271113(10)608740; 671500 (01)00880304461666(17)271030(10)671500; 671510 (01)00880304461666(17)280121(10)671510; 857040 (01)00880304461666(17)271112(10)857040;
Official Source
Always verify recall information with the official FDA source:
View on FDA.govFDA Recall Number: Z-0383-2024
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