Device recall
Z-2792-2018: MegaPower Electrosurgical Generator, Product code 1000, GTIN 10614559103715
FDA device recall · Class II · Megadyne Medical Products, Inc.
Key facts
| Recall number (Z-number) | Z-2792-2018 |
|---|---|
| Recall event | 80327 |
| Product | MegaPower Electrosurgical Generator, Product code 1000, GTIN 10614559103715 |
| Product code | GEI |
| Recalling firm | Megadyne Medical Products, Inc. |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Jan 30, 2024 |
| 510(k) numbers | K050579 |
| FEI number | 1721194 |
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