🔍 RecallPedia

AFT (Allograft Filler Tube) Diverted Tube (3/4 Filled), Product Code 227005 (bone void filler)

Class I - Dangerous
🏥 Medical Devices Recalled: December 22, 2023 Musculoskeletal Transplant Foundation Infusion Pumps

What Should You Do?

  1. Check if you have this product:
    UDI-DI: W4184227005T0473 Donor Lots 00322029241137 and 00322039641144
  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:
Musculoskeletal Transplant Foundation, Inc.
Reason for Recall:
Filling process qualification did not demonstrate adequate process capability. Possible consequences include extended surgery time due to extrudability issues.
Classification:
Class I - Dangerous

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

Status:
ongoing

Product Information

Full Description:

AFT (Allograft Filler Tube) Diverted Tube (3/4 Filled), Product Code 227005 (bone void filler)

Product Codes/Lot Numbers:

UDI-DI: W4184227005T0473 Donor Lots 00322029241137 and 00322039641144

Official Source

Always verify recall information with the official FDA source:

View on FDA.gov

FDA Recall Number: Z-1067-2024

Related Recalls