Musculoskeletal Transplant Foundation recalls AFT bone void filler tubes (Product Code 227010) that may cause extended surgery time due to extrudability issues. Affected units include specific donor lots and UDI-DI numbers.
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 because of issues with how the material flows during use. This affects medical procedures and requires attention to avoid delays.
The filler tubes may not flow properly during surgery, causing extended procedure times. This happens because the filling process wasn't tested well enough to ensure consistent performance.
Medical professionals using the AFT bone void filler tubes for surgeries are most at risk. Patients receiving this specific product during procedures may be affected.
Check for Product Code 227010 (bone void filler) with Donor Lot 02921115411127. The unique identifier is UDI-DI: W4184227010T0473.
Verify the Product Code 227010 and Donor Lot 02921115411127 on the tube.
The recall indicates possible extended surgery time due to extrudability issues, but no direct patient injury is mentioned.
Look for Product Code 227010 (bone void filler) with Donor Lot 02921115411127 and UDI-DI: W4184227010T0473.
The recall does not specify a stop-use instruction; only checking product details is mentioned.
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-1066-2024 — Musculoskeletal Transplant Foundation Musculoskeletal Transplant Foundation Hello, I own a Musculoskeletal Transplant Foundation that is covered by recall Z-1066-2024 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.
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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.
