Radiation therapy planning system may report overly high skin surface doses
RayStation versions 8.0.0.61 and 8.0.1.10 are subject to a Class II FDA recall due to a potential for calculated skin surface doses to be reported as too high. Healthcare facilities using these versions should contact the manufacturer for guidance and a corrective update.
- Product
- RayStation 8.0.0.61, 8.0.1.10. Radiation Therapy Treatment Planning System.
- Category
- Medical Device
- Distribution
- Distributed nationwide