⚠ RecallRadar📷 ScanGuidesOfficial U.S. recall notices, restated plainly

RAYSEARCH LABORATORIES AB: Brand Name: RayStation Product Name: RayStation/RayPlan Model/Catalog Number: 14.0.0, 15.0.0, 15.1.3 Software Version: RayStation 2023B,

Medical DevicesSource: FDA (device) · Date: 2026-01-28

Read the official notice at FDA (device) →

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The text below is copied from the official FDA (device) record. If anything differs, the official notice is correct.

Company / brand
RAYSEARCH LABORATORIES AB
Product
Brand Name: RayStation Product Name: RayStation/RayPlan Model/Catalog Number: 14.0.0, 15.0.0, 15.1.3 Software Version: RayStation 2023B, RayStation 2024A, RayStation 2024A SP3 Product Description: Radiation Therapy Treatment Planning System Component: No
Reason / hazard
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.
Classification
Class II
Status
Ongoing
Distribution / sold at
Refer to the attached documents: Distribution list 167168 US - updated, Distribution list 167168 OUS
Recall initiated
2025-11-28
Code info
Lot Code: UDI: 0735000201055620230630, 0735000201072320231213, 0735000201088420250129 GTIN: 07350002010556, 07350002010723, 07350002010884 Serial Numbers: 14.0.0.3338, 15.0.0.430, 15.1.3.10 Software Revisions: RayStation 2023B, RayStation 2024A, RayStation 2024A SP3 Expiration Date: 2030-02-21
Product quantity
119
Voluntary mandated
Voluntary: Firm initiated
City
Stockholm
Country
Sweden
Event id
98117
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