Device recall
Z-1874-2011: Toshiba Infinix-i, DFP-8000D The expected usage of these devices is for…
FDA device recall · Class II · Toshiba American Medical Systems Inc
Key facts
| Recall number (Z-number) | Z-1874-2011 |
|---|---|
| Recall event | 58134 |
| Product | Toshiba Infinix-i, DFP-8000D The expected usage of these devices is for fluoroscopy studies for various anatomical regions of the human body. |
| Product code | JAA |
| Recalling firm | Toshiba American Medical Systems Inc |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Mar 18, 2013 |
| FEI number | 2020563 |
At a glance
- None 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