Device recall
Z-1446-2020: Covidien Force TriVerse Electrosurgical Devices, Product numbers FT3000 and…
FDA device recall · Class II · Covidien Llc
Key facts
| Recall number (Z-number) | Z-1446-2020 |
|---|---|
| Recall event | 84991 |
| Product | Covidien Force TriVerse Electrosurgical Devices, Product numbers FT3000 and FT3000DB, UDI 10884524000084 20884524000081; 10884524001937 20884524001934 |
| Product code | GEI |
| Recalling firm | Covidien Llc |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Apr 26, 2024 |
| 510(k) numbers | K150735 |
| FEI number | 1282497 |
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