Device recall
Z-2684-2020: Nuvasive NVM5 EMG Module, REF 8020015, Rx ONLY, CE2797, Nonsterile, UDI…
FDA device recall · Class II · NuVasive Inc
Key facts
| Recall number (Z-number) | Z-2684-2020 |
|---|---|
| Recall event | 85889 |
| Product | Nuvasive NVM5 EMG Module, REF 8020015, Rx ONLY, CE2797, Nonsterile, UDI: 00887517206633 - Product Usage: is intended for intraoperative neurophysiologic monitoring during spinal surgery. |
| Product code | PDQ |
| Recalling firm | NuVasive Inc |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Mar 22, 2021 |
| 510(k) numbers | K143641 |
| FEI number | 3002980729 |
At a glance
- 1–9 Linked 510(k)s
- 1–9 Products in the same recall event
- 1–9 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