Device recall
Z-1460-2015: EOS, Digital radiography system used in general radiographic examinations.
FDA device recall · Class II · Eos Imaging Inc
Key facts
| Recall number (Z-number) | Z-1460-2015 |
|---|---|
| Recall event | 70732 |
| Product | EOS, Digital radiography system used in general radiographic examinations. |
| Product code | MQB |
| Recalling firm | Eos Imaging Inc |
| Recall class | Class II |
| Status | Terminated |
| Termination date | May 31, 2017 |
| 510(k) numbers | K123740 |
| FEI number | 3008632827 |
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