Musculoskeletal Transplant Foundation, Inc. recalls
Every recall we track for Musculoskeletal Transplant Foundation, Inc. — 5 in all, from 2019–2023 — plus the complaints and injury reports the public filed about them.
Recalls per year, by danger level
Recalls from Musculoskeletal Transplant Foundation, Inc. peaked in 2023 (3); 5 since 2017.
All FDA recall records for Musculoskeletal Transplant Foundation, Inc. since 2017, counted by recall date (one bar per calendar year; 2026 is partial). Danger level is GovInfoNow’s plain-language rating; “not yet rated” records are still being written up.
| Year | Stop using now | Use caution | Lower risk | Not yet rated | Total |
|---|---|---|---|---|---|
| 2017 | 0 | 0 | 0 | 0 | 0 |
| 2018 | 0 | 0 | 0 | 0 | 0 |
| 2019 | 0 | 0 | 1 | 0 | 1 |
| 2020 | 0 | 0 | 0 | 0 | 0 |
| 2021 | 0 | 0 | 1 | 0 | 1 |
| 2022 | 0 | 0 | 0 | 0 | 0 |
| 2023 | 0 | 0 | 3 | 0 | 3 |
| 2024 | 0 | 0 | 0 | 0 | 0 |
| 2025 | 0 | 0 | 0 | 0 | 0 |
| 2026 (to date) | 0 | 0 | 0 | 0 | 0 |
What to do if you have a recalled Musculoskeletal Transplant Foundation, Inc. product
- Match the model, catalog or lot number on your device to the recall.
- Ask the prescribing clinician or supplier what to do — many device recalls are corrections, not removals.
- Report problems to FDA MedWatch.
All Musculoskeletal Transplant Foundation, Inc. recalls
4 shown- Lower riskMedical device
Musculoskeletal Transplant Foundation, Inc. recalls AFT (Allograft Filler Tube) Straight Tube (1/2 Filled), Product Code 227010 (bone void filler)
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.
Musculoskeletal Transplant FoundationDec 22, 2023 - Lower riskMedical device
Musculoskeletal Transplant Foundation, Inc. recalls DBX Demineralized Bone Matrix Putty 10cc-Indicated for treatment of surgically created osseous defects or osseous
Musculoskeletal Transplant Foundation recalls DBX Demineralized Bone Matrix Putty labeled 10cc but actually 1cc. This may prolong surgery. Product model 038100 with specific serial numbers.
Musculoskeletal Transplant FoundationSep 22, 2023 - Lower riskMedical device
Musculoskeletal Transplant Foundation, Inc. recalls AFT Straight Tube (3/4 Filled) - Human Allograph Tissue for treatment of surgically-created osseous defects or osseous
Musculoskeletal Transplant Foundation recalls AFT Straight Tube (3/4 filled) due to potential surgery delay from improper filling. Affected units have specific lot numbers.
Musculoskeletal Transplant FoundationMar 29, 2021 - Lower riskMedical device
Musculoskeletal Transplant Foundation, Inc. recalls QuickGraft¿ Model # 430PST
Musculoskeletal Transplant Foundation recalls QuickGraft Model 430PST due to label measurements not accounting for tension, potentially increasing surgical time. Affected units have specific serial numbers listed.
Musculoskeletal Transplant FoundationAug 15, 2019
Musculoskeletal Transplant Foundation, Inc. recall questions
How many recalls has Musculoskeletal Transplant Foundation, Inc. had?
5 recalls from Musculoskeletal Transplant Foundation, Inc. are on record with U.S. safety agencies, from 2019–2023.
What is the most recent Musculoskeletal Transplant Foundation, Inc. recall?
Musculoskeletal Transplant Foundation, Inc. recalls AFT (Allograft Filler Tube) Straight Tube (1/2 Filled), Product Code 227010 (bone void filler), dated Dec 22, 2023. Every Musculoskeletal Transplant Foundation, Inc. recall is listed on this page, newest first.
What should I do if I have a recalled Musculoskeletal Transplant Foundation, Inc. product?
Match the model, catalog or lot number on your device to the recall. Ask the prescribing clinician or supplier what to do — many device recalls are corrections, not removals. Report problems to FDA MedWatch.
How do I get alerts for new Musculoskeletal Transplant Foundation, Inc. recalls?
Sign up for free email alerts on GovInfoNow — we check official CPSC, FDA, USDA and NHTSA data every day and email you only when a recall matches what you follow.