Device recall
Z-1455-2015: DBX Mix, 20 cc, Product Code: 058200. Demineralized Bone Matrix Mix, bone void…
FDA device recall · Class II · Musculoskeletal Transplant Foundation, Inc.
Key facts
| Recall number (Z-number) | Z-1455-2015 |
|---|---|
| Recall event | 70739 |
| Product | DBX Mix, 20 cc, Product Code: 058200. Demineralized Bone Matrix Mix, bone void filler. |
| Product code | MQV |
| Recalling firm | Musculoskeletal Transplant Foundation, Inc. |
| Recall class | Class II |
| Status | Terminated |
| Termination date | May 8, 2017 |
| 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