XP-XP Tibial Tray - Interlok 91mm Item # 195761

Class I - Dangerous

What Should You Do?

  1. Check if you have this product:
    Lot Number 183700 790980 202030 202020 202010 986220 986240 986240R 396520 986230 394870 394840 833310 394860 903470 508690 701050 701050R
  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-XP Tibial Tray - Interlok 91mm Item # 195761

Product Codes/Lot Numbers:

Lot Number 183700 790980 202030 202020 202010 986220 986240 986240R 396520 986230 394870 394840 833310 394860 903470 508690 701050 701050R

Distribution:

Nationwide distribution

Official Source

Always verify recall information with the official FDA source:

View on FDA.gov

FDA Recall Number: Z-2516-2019

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 →