Device recall
Z-2152-2017: Pausch Uroview FD fluoroscopic X-ray system UDI number (01)04260491620040…
FDA device recall · Class II · Hans Pausch Rontgengeratebau Gmbh
Key facts
| Recall number (Z-number) | Z-2152-2017 |
|---|---|
| Recall event | 76808 |
| Product | Pausch Uroview FD fluoroscopic X-ray system UDI number (01)04260491620040 Primarily for urological applications (functional X-ray diagnostics, endourology and minimal invasive urology / surgery). The system, which includes a radiologic / urologic treatment table, maybe used for urological treatment… |
| Product code | JAA |
| Recalling firm | Hans Pausch Rontgengeratebau Gmbh |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Jun 14, 2019 |
| 510(k) numbers | K161019 |
| FEI number | 3002807145 |
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