Device recall
Z-0890-2017: Best Practices kits containing certain production lots of Clearify Visualization…
FDA device recall · Class II · Medtronic
Key facts
| Recall number (Z-number) | Z-0890-2017 |
|---|---|
| Recall event | 75301 |
| Product | Best Practices kits containing certain production lots of Clearify Visualization System Item Code: 21-345 Intended to be used prior to and during endoscopic and laparoscopic procedures to prevent fogging of the scope as well as clean the scope lens |
| Product code | FEI |
| Recalling firm | Medtronic |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Aug 8, 2018 |
| 510(k) numbers | K062779 |
| FEI number | 1219930 |
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