Device recall
Z-0916-2012: Drystar Mammo. Display of Mammographic images.
FDA device recall · Class III · AGFA Corp.
Key facts
| Recall number (Z-number) | Z-0916-2012 |
|---|---|
| Recall event | 60762 |
| Product | Drystar Mammo. Display of Mammographic images. |
| Product code | IWZ |
| Recalling firm | AGFA Corp. |
| Recall class | Class III |
| Status | Terminated |
| Termination date | Feb 14, 2012 |
| FEI number | 3001236302 |
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