Discovery Elbow Humeral Trial Product Usage: Biomet manufactures a variety of elbow joint replacement prostheses intended for primary and revision joint arthoplasty for use in cemented applications. Elbow joint replacement components include humeral and ulnar components, and in some instances, hinge components.

Class I - Dangerous
🏥 Medical Devices Recalled: September 24, 2014 Biomet Implants & Prosthetics Nationwide

What Should You Do?

  1. Check if you have this product:
    Catalog Number: 414837 Lot Number: 555011
  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:
Biomet, Inc.
Reason for Recall:
An investigation identified that the product was incorrectly manufactured as a left humeral trial but is etched as a right humeral trial.
Classification:
Class I - Dangerous

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

Status:
terminated

Product Information

Full Description:

Discovery Elbow Humeral Trial Product Usage: Biomet manufactures a variety of elbow joint replacement prostheses intended for primary and revision joint arthoplasty for use in cemented applications. Elbow joint replacement components include humeral and ulnar components, and in some instances, hinge components.

Product Codes/Lot Numbers:

Catalog Number: 414837 Lot Number: 555011

Official Source

Always verify recall information with the official FDA source:

View on FDA.gov

FDA Recall Number: Z-0075-2015

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