Device recall
Z-1772-2020: Medivators Endo Smartcap Endoscope Tubing. REF100145. Packaged as Contents 1…
FDA device recall · Class II · Medivators, Inc.
Key facts
| Recall number (Z-number) | Z-1772-2020 |
|---|---|
| Recall event | 84109 |
| Product | Medivators Endo Smartcap Endoscope Tubing. REF100145. Packaged as Contents 1, 10, 50, and found in BMP-C145. Tubing for Olympus 140/240, 160/260, 180/280, 190/290 Series Endoscopes. Sterile EO - Product Usage: is intended to be used with an air or CO2 source and/or a pump along with a sterile water… |
| Product code | FAJ |
| Recalling firm | Medivators, Inc. |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Dec 11, 2020 |
| 510(k) numbers | K093665 |
| FEI number | 2150060 |
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