Device recall
Z-1166-2013: NeuViz Dual series CT Scanner System, Part number (PN): 989605651321. This is a…
FDA device recall · Class II · Philips And Neusoft Medical Systems Co., Ltd.
Key facts
| Recall number (Z-number) | Z-1166-2013 |
|---|---|
| Recall event | 64783 |
| Product | NeuViz Dual series CT Scanner System, Part number (PN): 989605651321. This is a computed X-ray, Tomography system. NeuViz Dual Multi-slice CT Scanner System is intended to produce cross-section images of head and body by computer reconstruction of X-ray transmission data taken at different angles. |
| Product code | JAK |
| Recalling firm | Philips And Neusoft Medical Systems Co., Ltd. |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Nov 22, 2013 |
| 510(k) numbers | K071308 |
| 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