Device recall
Z-2409-2024: NIM Vital Nerve Monitoring systems (all serial numbers manufactured) with NIM…
FDA device recall · Class I · Medtronic Xomed, Inc.
Key facts
| Recall number (Z-number) | Z-2409-2024 |
|---|---|
| Recall event | 94876 |
| Product | NIM Vital Nerve Monitoring systems (all serial numbers manufactured) with NIM Vital System versions: v1.0.0, v1.1.1, v1.3.2, v1.4.3. NIM Vital Nerve Integrity Monitor with below product descriptions. 1. CONSOLE NIM4CM01 NIM 4.0, Model Number: NIM4CM01. 2. CONSOLE NIM4CM01RF NIM 4.0 REFURBISHED… |
| Product code | GWF |
| Recalling firm | Medtronic Xomed, Inc. |
| Recall class | Class I |
| Status | Open, Classified |
| 510(k) numbers | K200759 |
| FEI number | 1045254 |
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