Device recall
Z-0738-2023: X-CORE 2 Ti Core, Static. Part of the NuVasive X-Core Expandable VBR System used…
FDA device recall · Class II · NuVasive Inc
Key facts
| Recall number (Z-number) | Z-0738-2023 |
|---|---|
| Recall event | 91196 |
| Product | X-CORE 2 Ti Core, Static. Part of the NuVasive X-Core Expandable VBR System used with spinal fixation. |
| Product code | MQP |
| Recalling firm | NuVasive Inc |
| Recall class | Class II |
| Status | Open, Classified |
| 510(k) numbers | K090176 |
| FEI number | 3002980729 |
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