Device recall
Z-0112-2014: Fujinon/Fujifilm Ultrasonic Endoscope Intended to provide ultrasonic images of…
FDA device recall · Class II · Fujinon Inc
Key facts
| Recall number (Z-number) | Z-0112-2014 |
|---|---|
| Recall event | 66144 |
| Product | Fujinon/Fujifilm Ultrasonic Endoscope Intended to provide ultrasonic images of submucosal and peripheral organs of the upper gastrointestinal tract for observation, diagnosis and endoscopic treatment. |
| Product code | FDS |
| Recalling firm | Fujinon Inc |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Mar 4, 2014 |
| 510(k) numbers | K120446 |
| FEI number | 2431293 |
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