Device recall
Z-1952-2012: CIVCO VirtuTRAX Instrument Navigator, Reusable non-sterile general purpose…
FDA device recall · Class II · Civco Medical Instruments Inc
Key facts
| Recall number (Z-number) | Z-1952-2012 |
|---|---|
| Recall event | 61793 |
| Product | CIVCO VirtuTRAX Instrument Navigator, Reusable non-sterile general purpose driveBAY, trakSTAR, electromagnetic sensor (8mm) with VirtuTRAX instrument navigator and (8.9 tapered to 1.3 x 147cm) telescopically-folded CIV-Flex sensor covers (5), Ref. 5350925. The firm name on the label is CIVCO… |
| Product code | IYO |
| Recalling firm | Civco Medical Instruments Inc |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Jan 7, 2015 |
| 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