--- title: "Musculoskeletal Transplant Foundation, Inc. Recalls: Agency-Reported Status and History (Oct 1, 2026) | Is It on Recall" description: "Search Musculoskeletal Transplant Foundation, Inc. recall records, lots, firms and dates. Reported status can be incomplete; use the linked agency notice for current instructions." url: https://isitonrecall.com/brand/musculoskeletal-transplant-foundation-inc/ updated: 2026-10-01 site: "Is It on Recall" language: en --- [Home](https://isitonrecall.com/) / Brand archive # Musculoskeletal Transplant Foundation, Inc. recall records **3** reported ongoing 3 records in this archive. Latest source date Dec 22, 2023. FDA enforcement status can lag behind the recall lifecycle. An empty search or a reported termination is not a personal product-safety determination. Archive changed Oct 1, 2026. USDA FSIS records are unavailable; [check FSIS directly](https://www.fsis.usda.gov/recalls). [Source coverage and dates](https://isitonrecall.com/sources/). ## Records and reported status Dec 22, 2023 FDA device enforcement ### [AFT (Allograft Filler Tube) Straight Tube (1/2 Filled), Product Code 227010 (bone void filler)](https://isitonrecall.com/recall/fda-device-z-1066-2024-aft-allograft-filler-tube-straight-tube-1-2-filled-product-code-227010-bone-void-filler/) Filling process qualification did not demonstrate adequate process capability. Possible consequences include extended surgery time due to extrudability issues. Class II Reported ongoing Distribution: Product was distributed to Minnesota. [Official source for AFT (Allograft Filler Tube) Straight Tube (1/2 Filled), Product Code 227010 (bone void filler)](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-1066-2024%22) Dec 22, 2023 FDA device enforcement ### [AFT (Allograft Filler Tube) Diverted Tube (3/4 Filled), Product Code 227005 (bone void filler)](https://isitonrecall.com/recall/fda-device-z-1067-2024-aft-allograft-filler-tube-diverted-tube-3-4-filled-product-code-227005-bone-void-filler/) Filling process qualification did not demonstrate adequate process capability. Possible consequences include extended surgery time due to extrudability issues. Class II Reported ongoing Distribution: Product was distributed to Minnesota. [Official source for AFT (Allograft Filler Tube) Diverted Tube (3/4 Filled), Product Code 227005 (bone void filler)](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-1067-2024%22) Sep 22, 2023 FDA device enforcement ### [DBX Demineralized Bone Matrix Putty 10cc-Indicated for treatment of surgically created osseous defects or osseous defects created from traumatic injury. Model Number: 038100](https://isitonrecall.com/recall/fda-device-z-0323-2024-dbx-demineralized-bone-matrix-putty-10cc-indicated-for-treatment-of-surgically-created-osseous-defec/) Units are labeled as 10cc; however the units have a fill volume of 1cc units. This may result in prolongation of surgery. Class II Reported ongoing Distribution: US Nationwide distribution in the states of PA, TX, WA. [Official source for DBX Demineralized Bone Matrix Putty 10cc-Indicated for treatment of surgically created osseous de...](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-0323-2024%22) ## Reasons in these listed records - Filling process qualification did not demonstrate adequate process capability. Possible consequences include extended surgery time due to extrudability issues. - Units are labeled as 10cc; however the units have a fill volume of 1cc units. This may result in prolongation of surgery. These examples come from this result page and are not a ranking of every recall reason. ## Checking Musculoskeletal Transplant Foundation, Inc. ### Is there a recall on musculoskeletal transplant foundation, inc. right now? This archive contains 3 records, including 3 with agency-reported ongoing status. The status field can be incomplete or stale. Open the current official notice and match your exact product. ### How do I check my package or product? Compare the product, firm and lot, date, model or serial identifiers with the notice. [Use the label-check guide](https://isitonrecall.com/guides/read-lot-codes/) if you need help locating an identifier. ### Does a matching name mean every item is included? A name is a search match. The agency notice sets the affected products and identifiers. Do not assume that every item with the same name or brand belongs to the recall. ### What if the search finds no matching record? This search has source and keyword limits. Missing records or a missing lot code do not establish that a product is unaffected. [Check source coverage](https://isitonrecall.com/sources/) and the agency's current notices. ### Where can I find older records? Use [monthly archives](https://isitonrecall.com/archives/) or the local search. The initial import covers records dated from October 2021 where available; each source's actual first and latest dates appear on the coverage page. ## Keep checking [Search Musculoskeletal Transplant Foundation, Inc.](https://isitonrecall.com/check/?q=Musculoskeletal%20Transplant%20Foundation%2C%20Inc.) [Browse related products](https://isitonrecall.com/products/) [Review source dates](https://isitonrecall.com/sources/)