Device recall
Z-2500-2018: Centron Product Usage: Vascular,cardiovascular and neurovascular imaging…
FDA device recall · Class II · Philips Healthcare
Key facts
| Recall number (Z-number) | Z-2500-2018 |
|---|---|
| Recall event | 80402 |
| Product | Centron Product Usage: Vascular,cardiovascular and neurovascular imaging applications,including diagnostic, interventional and minimally invasive procedures. Cardiac imaging applications including diagnostics, interventional and minimally invasive procedures (such as PTCA,stent… |
| Product code | OWB |
| Recalling firm | Philips Healthcare |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Jul 3, 2024 |
| FEI number | 1218950 |
At a glance
- None Linked 510(k)s
- 1–9 Products in the same recall event
- 100–999 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