Device recall
Z-1893-2017: Ziehm Imaging solo FD Mobile Fluoroscopic C-arm
FDA device recall · Class II · Ziehm Imaging Inc
Key facts
| Recall number (Z-number) | Z-1893-2017 |
|---|---|
| Recall event | 77030 |
| Product | Ziehm Imaging solo FD Mobile Fluoroscopic C-arm |
| Product code | OWB |
| Recalling firm | Ziehm Imaging Inc |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Dec 11, 2019 |
| 510(k) numbers | K161976 |
| FEI number | 2027299 |
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