Device recall
Z-0031-2022: Nox T3s Recorder - Product Usage: intended for ambulatory recording of…
FDA device recall · Class II · NOX MEDICAL
Key facts
| Recall number (Z-number) | Z-0031-2022 |
|---|---|
| Recall event | 88673 |
| Product | Nox T3s Recorder - Product Usage: intended for ambulatory recording of physiological signals during sleep. |
| Product code | MNR |
| Recalling firm | NOX MEDICAL |
| Recall class | Class II |
| Status | Terminated |
| Termination date | May 1, 2023 |
| 510(k) numbers | K082113 |
| FEI number | 3007389703 |
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