Musculoskeletal Transplant Foundation recalls AFT Diverted Tubes (Product Code 227005) that may cause extended surgery time due to extrudability issues. Affected units include specific donor lots.
Filling process qualification did not demonstrate adequate process capability. Possible consequences include extended surgery time due to extrudability issues.
Musculoskeletal Transplant Foundation recalls certain bone void filler tubes that could lead to longer surgery times. This is due to issues with how the tubes fill properly during medical procedures.
The filling process didn't work well enough to ensure the tubes fill correctly during surgery. This could cause delays in the procedure as the tube might not extrude properly.
Surgical teams using the recalled AFT Diverted Tubes (Product Code 227005) for bone void fillers are affected. Patients undergoing surgery with these tubes may experience longer procedures.
Check for Product Code 227005 (bone void filler) with UDI-DI: W4184227005T0473. Affected units include donor lots 00322029241137 and 00322039641144.
Verify the Product Code 227005 and UDI-DI: W4184227005T0473 on the tube packaging.
The filling process didn't demonstrate adequate capability, which could lead to extended surgery times due to extrudability issues.
The recall record does not specify a remedy, so contact the manufacturer directly for guidance.
Donor lots 00322029241137 and 00322039641144 are affected.
We’ve drafted a message you can send Musculoskeletal Transplant Foundation to request your refund or repair — edit it as you like.
Subject: Recall Z-1067-2024 — Musculoskeletal Transplant Foundation Musculoskeletal Transplant Foundation Hello, I own a Musculoskeletal Transplant Foundation that is covered by recall Z-1067-2024 from Musculoskeletal Transplant Foundation. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
Experiences, tips, and questions from readers. Every comment is reviewed before it appears.
No comments yet — be the first to share your experience.
The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
