Device recall
Z-1521-2022: NIM EMG Endotracheal Tube, Part Numbers: a) REF 8229307J b) REF 8229308J c) REF…
FDA device recall · Class I · Medtronic Xomed, Inc.
Key facts
| Recall number (Z-number) | Z-1521-2022 |
|---|---|
| Recall event | 90711 |
| Product | NIM EMG Endotracheal Tube, Part Numbers: a) REF 8229307J b) REF 8229308J c) REF 8229306J |
| Product code | ETN |
| Recalling firm | Medtronic Xomed, Inc. |
| Recall class | Class I |
| Status | Open, Classified |
| FEI number | 1045254 |
At a glance
- None 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