Device recall
Z-0493-03: Uroskop D1/D2/D3 - Table, Radiographic, Stationary Top.
FDA device recall · Class II · Siemens Medical Systems Inc
Key facts
| Recall number (Z-number) | Z-0493-03 |
|---|---|
| Recall event | 25329 |
| Product | Uroskop D1/D2/D3 - Table, Radiographic, Stationary Top. |
| Product code | IXR |
| Recalling firm | Siemens Medical Systems Inc |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Jan 10, 2005 |
| 510(k) numbers | K923049 |
| FEI number | 2240869 |
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