Device recall
Z-0494-05: X-Ray High Voltage Generator, Model KXO-80G used on Image Intensified…
FDA device recall · Class II · Toshiba American Med Sys Inc
Key facts
| Recall number (Z-number) | Z-0494-05 |
|---|---|
| Recall event | 31217 |
| Product | X-Ray High Voltage Generator, Model KXO-80G used on Image Intensified Fluoroscopoc X-Ray System DUA-450D |
| Product code | rad |
| Recalling firm | Toshiba American Med Sys Inc |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Feb 10, 2012 |
| FEI number | 2020563 |
At a glance
- None Linked 510(k)s
- 1–9 Products in the same recall event
- 1–9 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