Device recall
Z-2440-2015: ExacTrac 6.0.x Patient Positioning System, Radiation therapy. Intended to be…
FDA device recall · Class II · Brainlab AG
Key facts
| Recall number (Z-number) | Z-2440-2015 |
|---|---|
| Recall event | 71898 |
| Product | ExacTrac 6.0.x Patient Positioning System, Radiation therapy. Intended to be used to place patients at an accurately defined point within the treatment beam of a medical accelerator for stereotactic radiosurgery or radiotherapy procedures. |
| Product code | IYE |
| Recalling firm | Brainlab AG |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Jan 5, 2017 |
| 510(k) numbers | K120789 |
| 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