Device recall
Z-2237-2010: NeuViz Dual series Computed Tomography (CT) Scanner System, X-Ray System. Part…
FDA device recall · Class II · Neuisys, LLC
Key facts
| Recall number (Z-number) | Z-2237-2010 |
|---|---|
| Recall event | 49012 |
| Product | NeuViz Dual series Computed Tomography (CT) Scanner System, X-Ray System. Part Number: 989605651321. 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 | Neuisys, LLC |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Aug 23, 2010 |
| 510(k) numbers | K062451, K071308 |
| FEI number | 3004971655 |
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