Device recall
Z-2235-2008: NeuViz Dual series computed Tomography Scanner System, X-Ray System The CT…
FDA device recall · Class II · Philips And Neusoft Medical Systems Co., Ltd.
Key facts
| Recall number (Z-number) | Z-2235-2008 |
|---|---|
| Recall event | 48657 |
| Product | NeuViz Dual series computed Tomography Scanner System, X-Ray System The CT scanner is a whole body x-ray computed tomography scanner which features a continuously rotating tube-detector system and functions according to the fan beam principle. |
| Product code | JAK |
| Recalling firm | Philips And Neusoft Medical Systems Co., Ltd. |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Feb 16, 2012 |
| 510(k) numbers | K062451, 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