RaySearch Laboratories recalls specific versions of their radiation therapy software due to potential for reported SSD values to be too high, which could affect treatment accuracy.
Potential for reported SSD to be too high.
RaySearch Laboratories is recalling two versions of their RayStation radiation therapy software. The recall is due to a potential issue where the software might report an SSD (spherical surface distance) that is too high, which could lead to inaccurate radiation treatment planning.
The software might report an SSD (spherical surface distance) that is too high. This could lead to inaccurate radiation treatment planning, potentially affecting the precision of radiation doses delivered to patients.
Healthcare professionals using RaySearch Laboratories' RayStation software for radiation therapy treatment planning are likely affected. Patients receiving treatment with these specific software versions may be at risk if the SSD values are inaccurate.
Check for the software versions 9.0.0.113 and 9.0.1.142. The product was sold with UDI 0735000201017420190612 and 0735000201048820220420, GTIN 07350002010174 and 07350002010488, and serial numbers 9.0.0.113 and 9.0.1.142.
Verify your RayStation software version is not 9.0.0.113 or 9.0.1.142.
The recall is due to a potential issue where the software might report an SSD (spherical surface distance) that is too high, which could lead to inaccurate radiation treatment planning.
Check your software version. If it is 9.0.0.113 or 9.0.1.142, you should verify the version and contact RaySearch Laboratories for guidance.
The recall record does not mention a specific fix or remedy for this issue.
We’ve drafted a message you can send RaySearch Laboratories to request your refund or repair — edit it as you like.
Subject: Recall Z-1744-2024 — RaySearch Laboratories RaySearch Laboratories Hello, I own a RaySearch Laboratories that is covered by recall Z-1744-2024 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.
Experiences, tips, and questions from readers. Every comment is reviewed before it appears.
No comments yet — be the first to share your experience.
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.
