Device recall
Z-1259-2023: Brainlab ExacTrac Dynamic software, Medical Charged-Particle Radiation Therapy…
FDA device recall · Class II · Brainlab AG
Key facts
| Recall number (Z-number) | Z-1259-2023 |
|---|---|
| Recall event | 91664 |
| Product | Brainlab ExacTrac Dynamic software, Medical Charged-Particle Radiation Therapy System, model 20910-01E and 20910-01F. |
| Product code | IYE |
| Recalling firm | Brainlab AG |
| Recall class | Class II |
| Status | Open, Classified |
| 510(k) numbers | K220338 |
| FEI number | 3002619595 |
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