Device recall
Z-1228-2009: MEDRAD Sterile Disposable Syringe Kit, catalog number DSK 130-Q, Angiographic…
FDA device recall · Class II · Medrad Inc
Key facts
| Recall number (Z-number) | Z-1228-2009 |
|---|---|
| Recall event | 51495 |
| Product | MEDRAD Sterile Disposable Syringe Kit, catalog number DSK 130-Q, Angiographic Syringe for delivery of contrast media. |
| Product code | DXT |
| Recalling firm | Medrad Inc |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Jun 4, 2009 |
| FEI number | 2520313 |
At a glance
- None 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