RaySearch Laboratories recalls RayStation software versions 6.1.1.2 to 6.3.0.6 due to potential duplicate DICOM UIDs in radiation therapy systems. Affected units may cause data conflicts in treatment planning.
DICOM SOP Instance UID and Series Instance UID from RayGateway, i.e. the interface to Accuray's iDMS, are not guaranteed to be unique.
RaySearch Laboratories is recalling specific versions of their RayStation radiation therapy software. The software may create duplicate DICOM identifiers, which could cause treatment planning errors in radiation therapy systems.
The software may generate duplicate DICOM SOP Instance UIDs and Series Instance UIDs. This could cause data conflicts in radiation therapy treatment planning systems, potentially leading to incorrect treatment plans.
Radiation therapy professionals using RayStation software versions 6.1.1.2 through 6.3.0.6 are affected. Those using the software for treatment planning are most at risk of data conflicts.
Check if your RayStation software version is 6.1.1.2, 6.2.0.7, or 6.3.0.6. The unique device identifiers (UDIs) listed in the recall are 0735000201008220170529, 0735000201007520170630, and 0735000201024220190923.
Verify your RayStation software version by checking the version number in the software interface.
Reach out to RaySearch Laboratories for guidance on whether your version is affected and next steps.
The software may generate duplicate DICOM identifiers, which could cause data conflicts in radiation therapy treatment planning systems.
Software versions 6.1.1.2, 6.2.0.7, and 6.3.0.6 are affected.
Check your software version in the RayStation interface and compare it to the affected versions listed: 6.1.1.2, 6.2.0.7, or 6.3.0.6.
We’ve drafted a message you can send RaySearch Laboratories to request your refund or repair — edit it as you like.
Subject: Recall Z-2494-2025 — RaySearch Laboratories RaySearch Laboratories Hello, I own a RaySearch Laboratories that is covered by recall Z-2494-2025 from RaySearch Laboratories. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
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The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
