Device recall
Z-2325-2017: Video Cytoscopes
FDA device recall · Class II · Pentax of America Inc
Key facts
| Recall number (Z-number) | Z-2325-2017 |
|---|---|
| Recall event | 77310 |
| Product | Video Cytoscopes |
| Product code | EOQ |
| Recalling firm | Pentax of America Inc |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Mar 13, 2018 |
| 510(k) numbers | K131028, K131946 |
| FEI number | 1000080301 |
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