Device recall
Z-0154-06: Stellant CT Injection System. Powered Injector with Syringe. Angiographic…
FDA device recall · Class II · Medrad Inc
Key facts
| Recall number (Z-number) | Z-0154-06 |
|---|---|
| Recall event | 33846 |
| Product | Stellant CT Injection System. Powered Injector with Syringe. Angiographic Injector and Syringe. Model numbers S, SX, D, and DX |
| Product code | DXT |
| Recalling firm | Medrad Inc |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Aug 15, 2007 |
| 510(k) numbers | K023183, K033881 |
| FEI number | 2520313 |
At a glance
- 1–9 Linked 510(k)s
- 1–9 Products in the same recall event
- 10–99 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