RaySearch Laboratories recalls RayStation/RayPlan 9A software build 9.0.0.113 due to potential incorrect table position calculations during treatment planning. Affected users should contact the manufacturer for details.
There is a potential for erroneous propagation of the current tabletop positions when applying pitch or roll correction. Even though pitch and roll correction is never propagated, non-zero pitch or roll causes the lateral, longitudinal and vertical values propagated to be incorrect.
RaySearch Laboratories is recalling a specific version of their cancer treatment planning software. This version could cause incorrect table positions during radiation therapy planning, which might lead to inaccurate treatment delivery.
The software may incorrectly calculate table positions when applying pitch or roll corrections during radiation treatment planning. This could result in inaccurate treatment delivery if non-zero pitch or roll angles are used.
Medical professionals using RayStation/RayPlan 9A software build 9.0.0.113 for radiation treatment planning. Those who have this specific software version are most at risk.
Check if you have RayStation/RayPlan 9A software with build number 9.0.0.113. The unique device identifier (UDI) is 07350002010174.
Reach out to RaySearch Laboratories for specific instructions on how to verify your software version and next steps.
The recall indicates a potential for incorrect table position calculations during treatment planning, but the software is not considered immediately dangerous. Users should contact RaySearch Laboratories for details.
Contact RaySearch Laboratories to verify your software version and get instructions on next steps.
Check for build number 9.0.0.113 in RayStation/RayPlan software. The unique device identifier (UDI) is 07350002010174.
We’ve drafted a message you can send RaySearch Laboratories to request your refund or repair — edit it as you like.
Subject: Recall Z-1467-2020 — RaySearch Laboratories RaySearch Laboratories Hello, I own a RaySearch Laboratories that is covered by recall Z-1467-2020 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.
