Device recall
Z-0397-2022: VirtuTRAX Instrument Navigator, Sensor with 10 17 GA VirtutTRAX
FDA device recall · Class II · Civco Medical Instruments Co. Inc.
Key facts
| Recall number (Z-number) | Z-0397-2022 |
|---|---|
| Recall event | 88906 |
| Product | VirtuTRAX Instrument Navigator, Sensor with 10 17 GA VirtutTRAX |
| Product code | IYO |
| Recalling firm | Civco Medical Instruments Co. Inc. |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Sep 30, 2024 |
| 510(k) numbers | K092619 |
| FEI number | 1937223 |
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