Device recall
Z-0209-2024: Abbott NT2000iX Radiofrequency (RF) generator, REF RFG-NT-2000, lesioning…
FDA device recall · Class II · Abbott
Key facts
| Recall number (Z-number) | Z-0209-2024 |
|---|---|
| Recall event | 93152 |
| Product | Abbott NT2000iX Radiofrequency (RF) generator, REF RFG-NT-2000, lesioning generator |
| Product code | GXD |
| Recalling firm | Abbott |
| Recall class | Class II |
| Status | Open, Classified |
| 510(k) numbers | K111576 |
| FEI number | 3005334138 |
At a glance
- 1–9 Linked 510(k)s
- 1–9 Products in the same recall event
- 1–9 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