🔍 RecallPedia

MEDPOR Titan OFW - MTB - Right - 1.0mm, Catalog number 81032

Class I - Dangerous
🏥 Medical Devices Recalled: December 29, 2021 Stryker Leibinger GmbH & Co. KG Other Medical Devices Nationwide

What Should You Do?

  1. Check if you have this product:
    UDI: 07613252084334; Lot Number: 3R7YHD
  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:
Stryker Leibinger GmbH & Co. KG
Reason for Recall:
Inside the packaging of one reported item a non-conforming product was found. Contrary to the design, the barrier layer was manufactured on the inferior side of the implant versus the superior side.
Classification:
Class I - Dangerous

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

Status:
terminated

Product Information

Full Description:

MEDPOR Titan OFW - MTB - Right - 1.0mm, Catalog number 81032

Product Codes/Lot Numbers:

UDI: 07613252084334; Lot Number: 3R7YHD

Official Source

Always verify recall information with the official FDA source:

View on FDA.gov

FDA Recall Number: Z-0715-2022

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