Various trauma and sports medicine instruments and implants. Orthopedic manual surgical instrument.

Class I - Dangerous

What Should You Do?

  1. Check if you have this product:
    Part #'s 900728 900737 900738 900740 909836 110008343 110009769 231201303 Lot #'s 669220 625160 625180 679060 529190 585920 742460 751280 751290 751330 751400 751410 751420 751430 630570
  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:
Insufficient seal strength on sterile barrier packaging. The seal could be jeopardized causing the sterile barrier to be compromised and the product could become nonsterile. If the product becomes non-sterile and is used or implanted, it may lead to an infection.
Classification:
Class I - Dangerous

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

Status:
terminated

Product Information

Full Description:

Various trauma and sports medicine instruments and implants. Orthopedic manual surgical instrument.

Product Codes/Lot Numbers:

Part #'s 900728 900737 900738 900740 909836 110008343 110009769 231201303 Lot #'s 669220 625160 625180 679060 529190 585920 742460 751280 751290 751330 751400 751410 751420 751430 630570

Official Source

Always verify recall information with the official FDA source:

View on FDA.gov

FDA Recall Number: Z-1827-2016

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