Medical device recalls Moderate risk

RAYSEARCH LABORATORIES AB recalls Brand Name: RayStation Product Name: RayStation/RayPlan Model/Catalog Number: 15.2.0, 15.1.3 Software Version: RayStati…

Recall date
November 28, 2025
Source
U.S. Food & Drug Administration (FDA) — enforcement report
Recall number
Z-1108-2026
FDA classification
Class II
Brand / firm
RAYSEARCH LABORATORIES AB
Sold / distributed
Refer to the attached documents: Distribution list 167168 US - updated, Distribution list 167168 OUS

Why it was recalled

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.

Class II means using this product may cause temporary or medically reversible health problems; the chance of serious harm is remote.

What was recalled

Brand Name: RayStation Product Name: RayStation/RayPlan Model/Catalog Number: 15.2.0, 15.1.3 Software Version: RayStation 2024A SP1, RayStation 2024A SP2 Product Description: Radiation Therapy Treatment Planning System Component: No

Get recall alerts

Free email alert whenever RAYSEARCH LABORATORIES AB has a new recall — straight from official government data. Unsubscribe anytime.

More recalls from: RAYSEARCH LABORATORIES AB