Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
AFT (Allograft Filler Tube) Straight Tube (1/2 Filled) Recalled by Musculoskeletal Transplant Foundation, Inc. Due to Filling process qualification did not demonstrate adequate process...
What You Should Do
Stop using this product immediately. Do not consume, use, or distribute it.
Return the product to the place of purchase for a full refund. If you have questions, contact Musculoskeletal Transplant Foundation, Inc. directly.
Affected Products
AFT (Allograft Filler Tube) Straight Tube (1/2 Filled), Product Code 227010 (bone void filler)
Quantity: 89
Why Was This Recalled?
Filling process qualification did not demonstrate adequate process capability. Possible consequences include extended surgery time due to extrudability issues.
Where Was This Sold?
Product was distributed to Minnesota.
About Musculoskeletal Transplant Foundation, Inc.
Musculoskeletal Transplant Foundation, Inc. has 9 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report