RaySearch Laboratories recalls RayStation software versions 13.0.0.1547 and 13.1.x due to potential duplicate DICOM identifiers, which could cause treatment planning errors in radiation therapy. Affected users should contact the manufacturer for details.
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 because duplicate DICOM identifiers might cause treatment planning errors. This could lead to incorrect radiation doses being delivered to patients during cancer treatment.
The software may generate duplicate DICOM identifiers, which are unique codes used to track medical images. If these identifiers are not unique, the system might incorrectly link images, leading to inaccurate radiation treatment plans.
Users of RayStation software versions 13.0.0.1547, 13.1.0.144, and 13.1.1.89 are affected. Medical professionals using this software for radiation therapy planning are most at risk.
Check if your RayStation software version is 13.0.0.1547, 13.1.0.144, or 13.1.1.89. The software was sold between 2022 and 2028.
Review your RayStation software version to see if it matches the recalled versions: 13.0.0.1547, 13.1.0.144, or 13.1.1.89.
The hazard is that DICOM identifiers may not be unique, which could cause treatment planning errors in radiation therapy.
Check your RayStation software version; the recalled versions are 13.0.0.1547, 13.1.0.144, and 13.1.1.89.
The recall does not specify a remedy, so contact RaySearch Laboratories directly for guidance.
We’ve drafted a message you can send RaySearch Laboratories to request your refund or repair — edit it as you like.
Subject: Recall Z-2493-2025 — RaySearch Laboratories RaySearch Laboratories Hello, I own a RaySearch Laboratories that is covered by recall Z-2493-2025 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.
