Device recall
Z-2807-2015: EVIS EXERA II Duodenovideoscope OLYMPUS TJF TypeQ180V. This instrument has been…
FDA device recall · Class II · Olympus America Inc.
Key facts
| Recall number (Z-number) | Z-2807-2015 |
|---|---|
| Recall event | 70858 |
| Product | EVIS EXERA II Duodenovideoscope OLYMPUS TJF TypeQ180V. This instrument has been designed to be used with an Olympus video system center, light source, documentation equipment, monitors, EndoTherapy accessories (such as a biopsy forceps), and other ancillary equipment for endoscopy and endoscopic… |
| Product code | FDT |
| Recalling firm | Olympus America Inc. |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Feb 1, 2017 |
| 510(k) numbers | K080403 |
| FEI number | 2429304 |
At a glance
- 1–9 Linked 510(k)s
- 1–9 Products in the same recall event
- 10–99 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