Device recall
Z-0274-2008: Precision 500D Classical R&F System with control room PC; Image-intensified…
FDA device recall · Class II · GE Healthcare
Key facts
| Recall number (Z-number) | Z-0274-2008 |
|---|---|
| Recall event | 47235 |
| Product | Precision 500D Classical R&F System with control room PC; Image-intensified fluoroscopic x-ray system; ; Model Number: 5117866-27. |
| Product code | JAA |
| Recalling firm | GE Healthcare |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Sep 10, 2008 |
| 510(k) numbers | K011624 |
| 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