Device recall
Z-1861-2016: Endoscope ED-250XL5 Operations Manual: Cleaning, Disinfection
FDA device recall · Class II · Fujifilm Medical Systems U.S.A., Inc.
Key facts
| Recall number (Z-number) | Z-1861-2016 |
|---|---|
| Recall event | 73469 |
| Product | Endoscope ED-250XL5 Operations Manual: Cleaning, Disinfection |
| Product code | FDT |
| Recalling firm | Fujifilm Medical Systems U.S.A., Inc. |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Jan 18, 2018 |
| 510(k) numbers | K944759 |
| 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