Device recall
Z-1520-2022: NIM EMG Endotracheal Tube, Part Numbers: a) REF 8229308 b) REF 8229307 c) REF…
FDA device recall · Class I · Medtronic Xomed, Inc.
Key facts
| Recall number (Z-number) | Z-1520-2022 |
|---|---|
| Recall event | 90711 |
| Product | NIM EMG Endotracheal Tube, Part Numbers: a) REF 8229308 b) REF 8229307 c) REF 8229306 |
| Product code | ETN |
| Recalling firm | Medtronic Xomed, Inc. |
| Recall class | Class I |
| Status | Open, Classified |
| 510(k) numbers | K050162, K925640 |
| 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