ClearanceBrief
Recall Z-0732-2022 ยท MUJ System, Planning, Radiation Therapy Treatment

RAYSEARCH LABORATORIES AB

RayStation/RayPlan- designed for treatment planning and analysis of radiation therapy. Software Version: 6.0.0.24 , 6.1.0.26 , 6.1.1.2 , 6.2.0.7 , 6.3.0.6 , 7.0.0.19 , 8.0.0.61 , 8.0.1.10 , 8.1.0.47 , 8.1.1.8 , 8.1.2.5 , 9.0.0.113 , 9.1.0.933 , 9.2.0.483 . Including Service Paks: Product name (build number) UDI-DI RayStation 6/RayPlan 2 (6.0.0.24) 07350002010013 RayStation 6/RayPlan

DateDec 30, 2021
StatusOpen, Classified
ReasonIf a new primary image set is selected while the cine loop is running, the primary image set will be displayed as both primary and secondary image set in all side-by-side views. This will also be true for any new patient or case opened while the cine loop is running
Root causeSoftware design
ActionRaySearch issued Field Safety Notice, Medical Device Correction #90375 via E-mail, on 30 December 2021. Letter stated reason for recall, health risk and action to take: Do not change the primary image set while the cine loop is running. " If the primary image set has been changed while the cine loop is running, restart RayStation/RayPlan to restore correct behavior. " Educate planning staff and all users about this workaround. " Inspect your product and identify all installed units with the above software version number(s). " Confirm you have read and understood this notice by replying to the
Quantity75 Licenses
DistributionUS Nationwide distribution.
FDA recordOpen on fda.gov

510(k) clearances named in this recall

K211867RayStation 11.0
RaySearch Laboratories AB (PUBL), Sep 8, 2021