Device recall
Z-0323-2024: DBX Demineralized Bone Matrix Putty 10cc-Indicated for treatment of surgically…
FDA device recall · Class II · Musculoskeletal Transplant Foundation, Inc.
Key facts
| Recall number (Z-number) | Z-0323-2024 |
|---|---|
| Recall event | 93296 |
| 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 |
| Product code | MQV |
| Recalling firm | Musculoskeletal Transplant Foundation, Inc. |
| Recall class | Class II |
| Status | Open, Classified |
| 510(k) numbers | K040262 |
| FEI number | 3001236616 |
At a glance
- 1–9 Linked 510(k)s
- 1–9 Products in the same recall event
- 100–999 Recalled products with this product code
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About FDA device recalls (products)
Each recalled device product receives a Z-number. Recall details such as root cause, distribution and firm actions are available in Orca1.
Source: U.S. Food and Drug Administration (FDA), Medical Device Recalls database