RaySearch Laboratories recalls specific versions of RayStation 8.0 software due to potential for reported SSD values to be too high, which could affect radiation therapy treatment planning accuracy.
Potential for reported SSD to be too high.
RaySearch Laboratories is recalling specific versions of their RayStation 8.0 software for radiation therapy treatment planning. The recall is due to a potential issue where the software might report higher than expected SSD values, which could lead to inaccurate radiation treatments.
The software may report SSD (sagittal slice distance) values that are too high. This could lead to inaccurate radiation treatment planning, potentially affecting the precision of radiation doses delivered to patients.
Radiation therapy treatment planners and healthcare providers using RaySearch Laboratories' RayStation 8.0 software versions 8.0.0.61 and 8.0.1.10 are affected. Those using the software for radiation treatment planning are most at risk.
Check your software version in RayStation. Versions 8.0.0.61 and 8.0.1.10 are affected. The software was sold with specific serial numbers and expiration dates listed in the recall notice.
Verify your RayStation version by looking for the software version number in the application settings.
The recall is for potential inaccuracies in SSD values, which could affect treatment planning. However, the software is not immediately dangerous and the risk is considered low.
Check your software version. If you have versions 8.0.0.61 or 8.0.1.10, you should check with RaySearch Laboratories for the next steps.
Look for the software version numbers 8.0.0.61 or 8.0.1.10 in your RayStation application. The affected versions were sold with specific serial numbers and expiration dates listed in the recall notice.
We’ve drafted a message you can send RaySearch Laboratories to request your refund or repair — edit it as you like.
Subject: Recall Z-1742-2024 — RaySearch Laboratories RaySearch Laboratories Hello, I own a RaySearch Laboratories that is covered by recall Z-1742-2024 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.
