Device recall
Z-1270-2022: Philips OmniWire Pressure guide wire REF 89185J PN 300000252891
FDA device recall · Class II · Volcano Corp
Key facts
| Recall number (Z-number) | Z-1270-2022 |
|---|---|
| Recall event | 90292 |
| Product | Philips OmniWire Pressure guide wire REF 89185J PN 300000252891 |
| Product code | DXQ |
| Recalling firm | Volcano Corp |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Dec 23, 2024 |
| 510(k) numbers | K202543 |
| FEI number | 3008363989 |
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