TRIDENTII HEMI CLUSTER44B- Indicated for use in primary and revision patients at high risk of hip dislocation Catalog Number: 702-11-44B

Class I - Dangerous

What Should You Do?

  1. Check if you have this product:
    UDI-DI: (01)07613327380897(17)290313(10) Lot Number: 14974852
  2. Do not eat it: Even if it looks and smells fine, do not consume this product.
  3. Throw it away or return it: You can return the product to the store for a full refund.
  4. Seek medical attention if needed: If you've consumed this product and feel unwell, contact your doctor immediately.
  5. 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:
Howmedica Osteonics Corp.
Reason for Recall:
The acetabular shell may have excessive deburring, resulting in a smooth surface on the edge of the shell
Classification:
Class I - Dangerous

Dangerous or defective products that predictably could cause serious health problems or death.

Status:
ongoing

Product Information

Full Description:

TRIDENTII HEMI CLUSTER44B- Indicated for use in primary and revision patients at high risk of hip dislocation Catalog Number: 702-11-44B

Product Codes/Lot Numbers:

UDI-DI: (01)07613327380897(17)290313(10) Lot Number: 14974852

Official Source

Always verify recall information with the official FDA source:

View on FDA.gov

FDA Recall Number: Z-1621-2024

Related Recalls

Anterior locking tabs on the Triathlon Universal Baseplate are out of specification which may prevent engagement of either of the two locking tabs with the locking wire of the tibial insert.

Sep 4, 2024 Implants & Prosthetics Nationwide View Details →