Device recall
Z-0466-2013: NeuViz 16 Multi-Sliced CT Scanner System, part number 989605858501. NeuViz Dual…
FDA device recall · Class II · Philips And Neusoft Medical Systems Co., Ltd.
Key facts
| Recall number (Z-number) | Z-0466-2013 |
|---|---|
| Recall event | 63553 |
| Product | NeuViz 16 Multi-Sliced CT Scanner System, part number 989605858501. NeuViz Dual series CT Scanner System, part number 989605651321 The NeuViz 16 CT Scanner System can be used as a whole body computed tomography X-ray system featuring a continuously rotating X-ray tube and detector array with… |
| Product code | JAK |
| Recalling firm | Philips And Neusoft Medical Systems Co., Ltd. |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Jul 8, 2013 |
| 510(k) numbers | K062451, K071308, K090173, K092742 |
| FEI number | 3003575350 |
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