Device recall
Z-1519-2022: NIM CONTACT EMG Endotracheal Tube, Part Numbers: a) REF 8229508 b) REF 8229507…
FDA device recall · Class I · Medtronic Xomed, Inc.
Key facts
| Recall number (Z-number) | Z-1519-2022 |
|---|---|
| Recall event | 90711 |
| Product | NIM CONTACT EMG Endotracheal Tube, Part Numbers: a) REF 8229508 b) REF 8229507 c) REF 8229506 |
| Product code | ETN |
| Recalling firm | Medtronic Xomed, Inc. |
| Recall class | Class I |
| Status | Open, Classified |
| 510(k) numbers | K050162 |
| 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