Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Musculoskeletal Transplant Foundation Recalled by Musculoskeletal Transplant Foundation, Inc. Due to AFT Diverted Tubes are being recalled due to...
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
Musculoskeletal Transplant Foundation, AFT Diverted Tube (3/4/Filled), indicated for treatment of surgically-created osseous defects or osseous defects created from traumatic injury. It can be used in the: extremities, pelvis, and spine. Product Code: 227005.
Quantity: 114 units
Why Was This Recalled?
AFT Diverted Tubes are being recalled due to a customer complaint involving one unit which had an unsealed Tyvek pouch. The non-sterile foil pouch may introduce contamination into the sterile field.
Where Was This Sold?
This product was distributed nationwide across all 50 states.
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