Device recall
Z-0292-2008: Medrad Avanta Multi-Patient Disposable Hand Controller, Angiographic Injector…
FDA device recall · Class II · Medrad Inc
Key facts
| Recall number (Z-number) | Z-0292-2008 |
|---|---|
| Recall event | 45817 |
| Product | Medrad Avanta Multi-Patient Disposable Hand Controller, Angiographic Injector and Syringe. Catalog number AVA 500 HC, For Use with MEDRAD Avant Fluid Management System, MEDRAD, Inc., Indianola, PA 15051 |
| Product code | DXT |
| Recalling firm | Medrad Inc |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Apr 22, 2008 |
| 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