Device recall
Z-1020-2019: Covidien Force TriVerse electrosurgical device 10 cord-Intended as…
FDA device recall · Class II · Covidien, PLC
Key facts
| Recall number (Z-number) | Z-1020-2019 |
|---|---|
| Recall event | 82244 |
| Product | Covidien Force TriVerse electrosurgical device 10 cord-Intended as electrosurgical energy to cut and/or coagulate tissue. Product Usage: Single-use device intended for use in open procedures (such as general, urologic, thoracic, plastic and reconstructive, gynecologic) and minimally invasive… |
| Product code | GEI |
| Recalling firm | Covidien, PLC |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Jun 17, 2020 |
| 510(k) numbers | K150735 |
| FEI number | 1717344 |
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