Device recall
Z-2540-2017: Vue Optic Visualization Source, Flexor Vue Deflecting Endoscopic System…
FDA device recall · Class II · Cook Inc.
Key facts
| Recall number (Z-number) | Z-2540-2017 |
|---|---|
| Recall event | 77305 |
| Product | Vue Optic Visualization Source, Flexor Vue Deflecting Endoscopic System, Endoscope, Fiber Optic, Supplied sterilized by ethylene oxide gas in peel-open packages |
| Product code | FFS |
| Recalling firm | Cook Inc. |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Jan 26, 2018 |
| 510(k) numbers | K072521 |
| FEI number | 1820334 |
At a glance
- 1–9 Linked 510(k)s
- 1–9 Products in the same recall event
- 1–9 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