ClearanceBrief
Recall Z-1105-2026 ยท MUJ System, Planning, Radiation Therapy Treatment

RAYSEARCH LABORATORIES AB

Brand Name: RayStation Product Name: RayStation/RayPlan Model/Catalog Number: 13.0.0.1547, 13.1.0.144, 13.1.1.89 Software Version: RayStation 12A, RayStation 12A SP1, RayStation 12A SP2 Product Description: Radiation Therapy Treatment Planning System Component: No

DateJan 16, 2026 (initiated Nov 28, 2025)
StatusOpen, Classified
ReasonPotential 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.
Root causeUnder Investigation by firm
ActionRaySearch Laboratories notified consignees via email on about 12/05/2025. Consignees were instructed to follow the outlined steps in the notification letter when adding geometry to an empty ROI with MO or type Bolus, Fixation or Support, educate planning staff and all users about the workaround, inspect units and identify all installed units with the affected software version numbers, and confirm receipt and understanding of the customer notification by responding to the notification email. The issue will be resolved in the next version of RayStation, scheduled for market release in Decembe
Quantity8
DistributionRefer to the attached documents: Distribution list 167168 US - updated, Distribution list 167168 OUS
FDA recordOpen on fda.gov

510(k) clearances named in this recall

K222312RayStation 12A
RaySearch Laboratories AB (PUBL), Mar 29, 2023