Device recall
Z-2240-2021: Covidien Sonicision Reusable Generator-converts electrical power from the…
FDA device recall · Class II · Covidien Llc
Key facts
| Recall number (Z-number) | Z-2240-2021 |
|---|---|
| Recall event | 88271 |
| Product | Covidien Sonicision Reusable Generator-converts electrical power from the battery pack to ultrasonic energy to drive the active blade. Product Number: SCGAA |
| Product code | LFL |
| Recalling firm | Covidien Llc |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Jan 28, 2025 |
| 510(k) numbers | K180149 |
| 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