Device recall
Z-0563-2014: Ziehm Solo C-Arm Interventional Fluoroscopic X-Ray System. Mobile Fluoroscopic…
FDA device recall · Class II · Ziehm Imaging Inc
Key facts
| Recall number (Z-number) | Z-0563-2014 |
|---|---|
| Recall event | 66976 |
| Product | Ziehm Solo C-Arm Interventional Fluoroscopic X-Ray System. Mobile Fluoroscopic Imaging |
| Product code | OWB |
| Recalling firm | Ziehm Imaging Inc |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Jun 23, 2014 |
| 510(k) numbers | K092438 |
| 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