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 | Units are labeled as 10cc; however the units have a fill volume of 1cc units. This may result in prolongation of surgery. |
| Product | DBX Demineralized Bone Matrix Putty 10cc-Indicated for treatment of surgically created osseous defects or osseous defects created from traumatic injury. Model Number: 038100 |
| Quantity | 18 units |
| Distribution | US Nationwide distribution in the states of PA, TX, WA. |
| Initiated | 2023-09-22 |
| Classified | 2023-11-17 |
| Recall number | Z-0323-2024 |
| 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-0323-2024).” Compiled from U.S. FDA public records (openFDA; FDA Data Dashboard). Data as of 2026-10-06. https://regwarden.com/recall/93296/
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