Device recall
Z-2639-2016: Ziehm Vision RFD 3D Mobile C-arm for Mobile Fluoroscopic Imaging
FDA device recall · Class II · Ziehm Imaging Inc
Key facts
| Recall number (Z-number) | Z-2639-2016 |
|---|---|
| Recall event | 74013 |
| Product | Ziehm Vision RFD 3D Mobile C-arm for Mobile Fluoroscopic Imaging |
| Product code | OWB |
| Recalling firm | Ziehm Imaging Inc |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Jul 18, 2019 |
| 510(k) numbers | K142740 |
| 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