RaySearch Laboratories recalls RayStation 7.0.0.19 radiation therapy software due to potential for reported SSD (safety distance) values to be too high, which could affect treatment accuracy.
Potential for reported SSD to be too high.
RaySearch Laboratories is recalling their RayStation 7.0.0.19 radiation therapy treatment planning software because it may report safety distances (SSD) that are too high. This could lead to inaccurate radiation treatments if not corrected.
The software may report safety distances (SSD) that are too high. This could cause radiation treatments to be less precise than intended, potentially affecting treatment outcomes. However, the risk is not immediate or severe under normal use conditions.
Radiation therapy professionals who use RayStation 7.0.0.19 software for treatment planning are likely affected. Patients receiving radiation therapy through this software may be at risk if the SSD values are inaccurate.
Check for the software version 7.0.0.19. The product was sold with a specific serial number format (7.0.0.19) and an expiration date of October 4, 2022.
Verify if your RayStation software version is 7.0.0.19 by checking the software's version number.
The recall is for the software used by radiation therapy professionals. Patients are not directly affected unless their treatment is impacted by inaccurate software settings.
Check if your software version is 7.0.0.19. If so, you may need to update to a newer version or contact RaySearch Laboratories for guidance.
The recall record does not specify a deadline for action.
We’ve drafted a message you can send RaySearch Laboratories to request your refund or repair — edit it as you like.
Subject: Recall Z-1741-2024 — RaySearch Laboratories RaySearch Laboratories Hello, I own a RaySearch Laboratories that is covered by recall Z-1741-2024 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.
