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 | Terminated |
| Reason | 3/4 AFT Straight Fill Tubes (227007) filled only 1/2 way instead of 3/4, may cause delay of surgery |
| Product | AFT Straight Tube (3/4 Filled) - Human Allograph Tissue for treatment of surgically-created osseous defects or osseous defects created from traumatic injury. It can be used in the: extremities, pelvis, and spine Item Number: 227007 |
| Quantity | 672 units |
| Distribution | US Nationwide distribution in the state of MN. |
| Initiated | 2021-03-29 |
| Classified | 2021-05-12 |
| Terminated | 2023-04-27 |
| Recall number | Z-1562-2021 |
| 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-1562-2021).” Compiled from U.S. FDA public records (openFDA; FDA Data Dashboard). Data as of 2026-10-06. https://regwarden.com/recall/87677/
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