RAYSEARCH LABORATORIES AB: Device Recall
Recall #Z-1102-2026 · 11/28/2025
Class II: Risk
Recall Details
- Recall Number
- Z-1102-2026
- Classification
- Class II
- Product Type
- Device
- Recalling Firm
- RAYSEARCH LABORATORIES AB
- Status
- Ongoing
- Date Initiated
- 11/28/2025
- Location
- Stockholm, Sweden
- Voluntary/Mandated
- Voluntary: Firm initiated
- Product Quantity
- 0
Reason for Recall
Potential for the invalidation for calculated radiation dose does not work as intended for certain Regions of Interest (ROIs). This issue occurs for some ROI(s) which have no contours and either have a material override defined, or are of type Bolus, Fixation, or Support. In these cases, adding geometry to the ROI, subsequently modifying geometry, or removing the material override does not invalidate dose as intended.
Product Description
RayStation/RayPlan. Model/Catalog Number: 10.1. Software Version: RayStation/RayPlan 10B. Radiation Therapy Treatment Planning System
Distribution Pattern
Refer to the attached documents: Distribution list 167168 US - updated, Distribution list 167168 OUS
Other Recalls by RAYSEARCH LABORATORIES AB
- Class II: Risk 11/28/2025
- Class II: Risk 11/28/2025
- Class II: Risk 11/28/2025
- Class II: Risk 11/28/2025
- Class II: Risk 11/28/2025
Data from FDA openFDA enforcement reports. This site is not affiliated with or endorsed by the FDA. Recall information may be updated by the FDA at any time.