🔍 RecallPedia

M/DN Intramedullary Fixation 4.2 mm Diameter Cortical Screw, 3.5 mm Hex Head, 45 mm Length 00225304542 M/DN Intramedullary Fixation 4.2 mm Diameter Cortical Screw, 3.5 mm Hex Head, 70 mm Length 00225307042

Class I - Dangerous
🏥 Medical Devices Recalled: May 4, 2016 Zimmer Manufacturing B.V. Diagnostic Equipment Nationwide

What Should You Do?

  1. Check if you have this product:
    LOTS: 63295051 63293672
  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 Manufacturing B.V.
Reason for Recall:
A small hole may be present in the inner tray of specific lots of sterile Hip and Trauma Implant Screws.
Classification:
Class I - Dangerous

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

Status:
terminated

Product Information

Full Description:

M/DN Intramedullary Fixation 4.2 mm Diameter Cortical Screw, 3.5 mm Hex Head, 45 mm Length 00225304542 M/DN Intramedullary Fixation 4.2 mm Diameter Cortical Screw, 3.5 mm Hex Head, 70 mm Length 00225307042

Product Codes/Lot Numbers:

LOTS: 63295051 63293672

Official Source

Always verify recall information with the official FDA source:

View on FDA.gov

FDA Recall Number: Z-1678-2016

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