Device recall
Z-1062-2012: Agfa DX-D Imaging Package - (The detector power cables described in the Report…
FDA device recall · Class II · AGFA Corp.
Key facts
| Recall number (Z-number) | Z-1062-2012 |
|---|---|
| Recall event | 61052 |
| Product | Agfa DX-D Imaging Package - (The detector power cables described in the Report of Correction and Removal are connected to portable detector panels used in the DX-D systems) Product Usage: DX-D Imaging Package ha the same intended use as the predicative devices: namely to provide diagnostic quality… |
| Product code | MQB |
| Recalling firm | AGFA Corp. |
| Recall class | Class II |
| Status | Terminated |
| Termination date | May 10, 2012 |
| 510(k) numbers | K092669 |
| FEI number | 3001236302 |
At a glance
- 1–9 Linked 510(k)s
- 1–9 Products in the same recall event
- 100–999 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