Device recall
Z-1693-2015: Neusoft NeuViz 64 Multi-slice CT Scanner System
FDA device recall · Class II · Neusoft Medical System Co
Key facts
| Recall number (Z-number) | Z-1693-2015 |
|---|---|
| Recall event | 71306 |
| Product | Neusoft NeuViz 64 Multi-slice CT Scanner System |
| Product code | JAK |
| Recalling firm | Neusoft Medical System Co |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Dec 5, 2016 |
| 510(k) numbers | K121792 |
| FEI number | 3012244921 |
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