Zimmer Segmental Systems; Polyethylene Inserts, Size C. Knee replacement.

Class I - Dangerous

What Should You Do?

  1. Check if you have this product:
    Part numbers 00-5850-013-95
  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.

āš ļø Emergency: If you experience severe symptoms after consuming this product, call 911 or Poison Control at 1-800-222-1222.

Recall Details

Company:
Zimmer, Inc.
Reason for Recall:
After evaluation of 13 complaints(0.4% rate) for hyper-extension of the Zimmer Segmental System, Zimmer is updating the related surgical technique and instructions for use to provide additional instructions and patient conditions that may place excessive loading on the polyethylene insert.
Classification:
Class I - Dangerous

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

Status:
terminated

Product Information

Full Description:

Zimmer Segmental Systems; Polyethylene Inserts, Size C. Knee replacement.

Product Codes/Lot Numbers:

Part numbers 00-5850-013-95

Official Source

Always verify recall information with the official FDA source:

View on FDA.gov

FDA Recall Number: Z-0784-2014

Related Recalls

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Sep 26, 2025 Implants & Prosthetics Nationwide View Details →

Zimmer Biomet is conducting a medical device recall for two (2) lots of the Dual Mobility Vivacit-EĀæ Bearing due to a commingle. The outer package is labeled as a Size F 44 mm, however, the implant inside the package is a Size G 46 mm, and vice versa.

Sep 26, 2025 Implants & Prosthetics Nationwide View Details →