Device recall
Z-1064-2015: Digital Mobile X-ray Systems used to take diagnostic radiographic exposures or…
FDA device recall · Class II · Virtual Imaging, Inc.
Key facts
| Recall number (Z-number) | Z-1064-2015 |
|---|---|
| Recall event | 69388 |
| Product | Digital Mobile X-ray Systems used to take diagnostic radiographic exposures or patients. |
| Product code | IZL |
| Recalling firm | Virtual Imaging, Inc. |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Feb 20, 2018 |
| 510(k) numbers | K101517 |
| FEI number | 3011066290 |
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