Class II — Musculoskeletal Transplant Foundation, Inc.
| Recalling firm | MUSCULOSKELETAL TRANSPLANT FOUNDATION |
|---|---|
| Registered facility | View this company's 3 registered facilities → (openFDA recall records do not name a specific facility) |
| Classification | Class II |
| Status | Ongoing |
| Reason | Filling process qualification did not demonstrate adequate process capability. Possible consequences include extended surgery time due to extrudability issues. |
| Product | AFT (Allograft Filler Tube) Straight Tube (1/2 Filled), Product Code 227010 (bone void filler) |
| Quantity | 89 |
| Distribution | Product was distributed to Minnesota. |
| Initiated | 2023-12-22 |
| Classified | 2024-02-09 |
| Recall number | Z-1066-2024 |
| Initiation | Voluntary: Firm initiated |
Source: U.S. FDA via openFDA (opens in a new tab) (device registration & enforcement). Data as of 2026-10-06. Verify this recall record at FDA → (opens in a new tab)
Cite this record
RegWarden. “Class II recall — Musculoskeletal Transplant Foundation, Inc. (Z-1066-2024).” Compiled from U.S. FDA public records (openFDA; FDA Data Dashboard). Data as of 2026-10-06. https://regwarden.com/recall/93853/
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