Device recall
Z-1836-2017: Valleylab Laparoscopic Handset; Material # E2750; Laproscopic Handset…
FDA device recall · Class II · COVIDIEN MEDTRONIC
Key facts
| Recall number (Z-number) | Z-1836-2017 |
|---|---|
| Recall event | 76384 |
| Product | Valleylab Laparoscopic Handset; Material # E2750; Laproscopic Handset Non-Sterile Bulk; Material # E2750NSB Product Usage: For use in 5mm cannulas or larger cannulas with 5mm adapters during laparoscopic and thorascopic procedures. For use with a minimum peak voltage of 3625V. |
| Product code | GEI |
| Recalling firm | COVIDIEN MEDTRONIC |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Aug 8, 2018 |
| 510(k) numbers | K964175 |
| FEI number | 1219930 |
At a glance
- 1–9 Linked 510(k)s
- 1–9 Products in the same recall event
- 100–999 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