Device recall
Z-1447-2020: Kits containing Covidien Force TriVerse Electrosurgical Devices. Distributed in…
FDA device recall · Class II · Covidien Llc
Key facts
| Recall number (Z-number) | Z-1447-2020 |
|---|---|
| Recall event | 84991 |
| Product | Kits containing Covidien Force TriVerse Electrosurgical Devices. Distributed in EMEA (Europe, Middle East, and Africa) only. No US distribution. Kits are manufactured in The Netherlands. Item codes BREASTKIT01 BREASTKIT01 BREASTKIT01 BREASTKIT01 BREASTKIT01 BREASTKIT01 BREASTKIT01 BREASTKIT01… |
| Product code | GEI |
| Recalling firm | Covidien Llc |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Apr 26, 2024 |
| FEI number | 1282497 |
At a glance
- None 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