Device recall
Z-2072-2012: EOS X-ray Medical Diagnostic, X-ray Equipment System Digital Radiography used…
FDA device recall · Class II · Eos Imaging Inc
Key facts
| Recall number (Z-number) | Z-2072-2012 |
|---|---|
| Recall event | 62621 |
| Product | EOS X-ray Medical Diagnostic , X-ray Equipment System Digital Radiography used in general radiographic examination. |
| Product code | MQB |
| Recalling firm | Eos Imaging Inc |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Sep 16, 2013 |
| FEI number | 3008632827 |
At a glance
- None 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