Device recall
Z-2024-2021: Vivorte Trabexus EB 10 cc Bone Void Filler -Fill bone and/or defect in skeletal…
FDA device recall · Class II · Vivorte, Inc.
Key facts
| Recall number (Z-number) | Z-2024-2021 |
|---|---|
| Recall event | 88165 |
| Product | Vivorte Trabexus EB 10 cc Bone Void Filler -Fill bone and/or defect in skeletal system Model Number: 130703-10 |
| Product code | MBP |
| Recalling firm | Vivorte, Inc. |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Nov 17, 2021 |
| 510(k) numbers | K130703, K143547 |
| FEI number | 3010642815 |
At a glance
- 1–9 Linked 510(k)s
- 1–9 Products in the same recall event
- 10–99 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