Device recall
Z-0897-04: Advantx 1 LC1 Model 45258230 Angiographic X-ray System
FDA device recall · Class II · General Electric Med Systems
Key facts
| Recall number (Z-number) | Z-0897-04 |
|---|---|
| Recall event | 28747 |
| Product | Advantx 1 LC1 Model 45258230 Angiographic X-ray System |
| Product code | IZI |
| Recalling firm | General Electric Med Systems |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Jul 24, 2006 |
| 510(k) numbers | K890348 |
| FEI number | 2126677 |
At a glance
- 1–9 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