Lower riskMedical device recall · FDA · Published December 22, 2023
Musculoskeletal Transplant Foundation recalls AFT bone void filler tubes due to surgery
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.
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Contact the company
📍Recalling firmMusculoskeletal Transplant Foundation, Inc.125 May St Ste 300 · Edison, NJ 08837-3264
“Musculoskeletal Transplant Foundation recalls AFT bone void filler tubes due to surgery.” GovInfoNow, updated August 19, 2026. https://govinfonow.com/recall/56480-musculoskeletal-transplant-foundation-recalls-aft-bone-void-filler-tubes-due. Based on FDA recall #Z-1066-2024 (https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-1066-2024%22&limit=1).
The FDA announced on 2023-12-22 that Musculoskeletal Transplant Foundation, Inc. is recalling the AFT Straight Tube bone void filler due to inadequate process qualification that may cause extended surgery time.
The filling process qualification did not demonstrate adequate process capability, according to the FDA. Possible consequences include extended surgery time due to extrudability issues.
Context
GovInfoNow's records show Musculoskeletal Transplant Foundation, Inc. has 3 other recalls on record since 2019-08-15. Other recent recalls of similar products include DBX Bone Putty (2023-09-22), AFT Straight Tube (2021-03-29), and QuickGraft Model 430PST (2019-08-15). Other recent recalls of similar products include Orthorebirth BioCera Fibers Bone Filler (2026-03-25), Orthorebirth ZENBONE Bone Filler (2026-03-25), and F & A Foundation Reign Medical Clench Staple System (2026-07-15).
How to tell if you have this one
Check for Product Code 227010 (bone void filler) with Donor Lot 02921115411127. The unique identifier is UDI-DI: W4184227010T0473.
Brand
Musculoskeletal Transplant Foundation
Category
Medical device
FDA recall event · 2 products
All 2 products in this recall
FDA lists each product line separately under one recall event. Check your product description, lot or code numbers against each row. Every row shares the hazard and remedy on this page.
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.
Official source: FDA Recall #Z-1066-2024 (December 22, 2023) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for Z-1066-2024 to see it in context.
Plain-language summary written by qwen3:4b on August 19, 2026, from the official record above. Not reviewed by a person — if it conflicts with the FDA notice, the notice is correct. Report an error on this page.
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