Device recall
Z-0367-2011: MEDRAD Sterile Disposable Syringe Kit Recall, Catalog Number 150-FT-Q; Kit…
FDA device recall · Class II · Medrad Inc
Key facts
| Recall number (Z-number) | Z-0367-2011 |
|---|---|
| Recall event | 55839 |
| Product | MEDRAD Sterile Disposable Syringe Kit Recall, Catalog Number 150-FT-Q; Kit includes angiographic injector and syringe The contents of the package are intended to be used in the delivery of contrast media. |
| Product code | DXT |
| Recalling firm | Medrad Inc |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Nov 17, 2010 |
| FEI number | 3006316319 |
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