Device recall
Z-0644-2016: Model NuCARTGN. The NuCART is a mobile display and image management platform…
FDA device recall · Class II · CompView Medical, LLC
Key facts
| Recall number (Z-number) | Z-0644-2016 |
|---|---|
| Recall event | 72915 |
| Product | Model NuCARTGN. The NuCART is a mobile display and image management platform used in Minimally Invasive Surgery (MIS) environments to facilitate the routing and ergonomic display of video signals from source devices to flat-panel monitors. It is tailored for use with an OEC C-arm and Endo-Cam in MIS… |
| Product code | LMD |
| Recalling firm | CompView Medical, LLC |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Mar 31, 2016 |
| FEI number | 3006293618 |
At a glance
- None Linked 510(k)s
- 1–9 Products in the same recall event
- 10–99 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