RaySearch Laboratories recalls RayStation/RayPlan 8B software build 8.1.0.47 due to potential incorrect table position propagation during pitch/roll corrections. Affected users should contact for remedy.
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 RayStation/RayPlan 8B software version 8.1.0.47 because it may incorrectly calculate table positions when applying pitch or roll corrections. This could lead to inaccurate radiation treatment planning in medical settings.
The software may incorrectly propagate lateral, longitudinal, and vertical table positions when pitch or roll corrections are applied. This could result in inaccurate radiation treatment delivery if the software is used without proper validation.
Medical professionals using RayStation/RayPlan 8B software version 8.1.0.47 for radiation treatment planning. Those most at risk are clinicians who rely on precise table positioning during radiation therapy.
Check for the software version 8B, build number 8.1.0.47. The unique device identifier (UDI) is 07350002010129. This software is used for radiation treatment planning in medical facilities.
Reach out to RaySearch Laboratories for guidance on the recall and potential remedies.
RayStation/RayPlan 8B, build number 8.1.0.47.
The error may cause incorrect table position calculations during pitch or roll corrections, potentially leading to inaccurate radiation treatment delivery.
The recall record does not specify a fix or remedy.
We’ve drafted a message you can send RaySearch Laboratories to request your refund or repair — edit it as you like.
Subject: Recall Z-1464-2020 — RaySearch Laboratories RaySearch Laboratories Hello, I own a RaySearch Laboratories that is covered by recall Z-1464-2020 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.
