XP-CR Tibial Tray - Interlok 91 mm Item # 195279

Class I - Dangerous

What Should You Do?

  1. Check if you have this product:
    Lot Number 262480 960510 274400 274430 336060 336060R 274390 274410 279280 394540 394590 394570 821400 903420 960530 422490 512590
  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:
Zimmer Biomet, Inc.
Reason for Recall:
The locking bar not fully engaging
Classification:
Class I - Dangerous

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

Status:
terminated

Product Information

Full Description:

XP-CR Tibial Tray - Interlok 91 mm Item # 195279

Product Codes/Lot Numbers:

Lot Number 262480 960510 274400 274430 336060 336060R 274390 274410 279280 394540 394590 394570 821400 903420 960530 422490 512590

Distribution:

Nationwide distribution

Official Source

Always verify recall information with the official FDA source:

View on FDA.gov

FDA Recall Number: Z-2514-2019

Related Recalls

Zimmer Biomet is conducting a medical device correction to update the Instructions for Use (IFU) and the Surgical Techniques for the Polaris Spinal System Translation Screw and Cypher MIS Screw System. Users should be aware that changes were made to the contraindications section indicating that the Translation Screws should not be used with a direct current stimulation, as a high probability of construct failure exists when using Translation Screws containing CoCr with direct current simulation system.

Nov 17, 2020 Other Medical Devices Nationwide View Details →