RAYSEARCH LABORATORIES AB: Device Recall

Recall #Z-1104-2026 · 11/28/2025

Class II: Risk

Recall Details

Recall Number
Z-1104-2026
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
22 units

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 Numbers: 12.0.0, 12.1.0, 12.0.3, 12.0.4, 12.3.0. Software Version: RayStation 11B, RayStation 11B SP1, RayStation 11B SP2, RayStation 11B SP3, RayStation 11B SPT1. 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

View all recalls by RAYSEARCH LABORATORIES AB →

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.