🔍 RecallPedia

stryker ORTHOLOC 3Di Fusion Plate MTP Right, REF 58A221RT, bone stabilization and fixation

Class I - Dangerous
🏥 Medical Devices Recalled: April 10, 2023 Wright Medical Technology Other Medical Devices Nationwide

What Should You Do?

  1. Check if you have this product:
    UDI/DI 00889797101035, Lot Number 1737413
  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:
Wright Medical Technology, Inc.
Reason for Recall:
Two lots of Ortholoc 3Di Fusion plates contain incorrect dorsiflexion descriptions laser marked on the parts.
Classification:
Class I - Dangerous

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

Status:
ongoing

Product Information

Full Description:

stryker ORTHOLOC 3Di Fusion Plate MTP Right, REF 58A221RT, bone stabilization and fixation

Product Codes/Lot Numbers:

UDI/DI 00889797101035, Lot Number 1737413

Official Source

Always verify recall information with the official FDA source:

View on FDA.gov

FDA Recall Number: Z-1467-2023

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