Magna-Fx Cannulated Screw Fixation System Bone Screw Fully Threaded Sterile zimmer

Class I - Dangerous

What Should You Do?

  1. Check if you have this product:
    Item Number 00-1146-030,035, 040, 045, 050, 055, 060, 065, 070, 075, 080, 085, 090, 095, -99
  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:
Zimmer is recalling various trauma screws that failed a leak test due to damage of the inner cavity only.
Classification:
Class I - Dangerous

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

Status:
terminated

Product Information

Full Description:

Magna-Fx Cannulated Screw Fixation System Bone Screw Fully Threaded Sterile zimmer

Product Codes/Lot Numbers:

Item Number 00-1146-030,035, 040, 045, 050, 055, 060, 065, 070, 075, 080, 085, 090, 095, -99

Distribution:

Nationwide distribution

Official Source

Always verify recall information with the official FDA source:

View on FDA.gov

FDA Recall Number: Z-2244-2014

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 →