Device recall
Z-2833-2016: TriFoillmaging Triumph/Triumph II Research CT scanners.
FDA device recall · Class II · Northridge Tri-Modality Imaging,
Key facts
| Recall number (Z-number) | Z-2833-2016 |
|---|---|
| Recall event | 74838 |
| Product | TriFoillmaging Triumph/Triumph II Research CT scanners. |
| Product code | JAK |
| Recalling firm | Northridge Tri-Modality Imaging, |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Oct 6, 2016 |
| FEI number | 3010878127 |
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