RayStation/RayPlan 8A, Build Number 8.0.0.61, stand-alone software treatment planning system
Check against the official notice below — it lists the full affected range.
RaySearch Laboratories AB has recalled RayStation/RayPlan 8A, Build Number 8.0.0.61, a stand-alone software treatment planning system. The recalled system has a defect where applying pitch or roll correction can cause incorrect propagation of tabletop positions. Specifically, when pitch or roll values are non-zero, the lateral, longitudinal, and vertical position values that are propagated become inaccurate, even though the pitch and roll correction itself is not propagated. One system with UDI 07350002010112 was distributed to Tennessee.
The recall record does not specify a remedy or any recommended actions for affected consumers.
Written by software from the official notice below. Not reviewed by a lawyer.
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.
Reason for recall: 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. Distribution: The products were distributed to the following US states: TN Quantity: 1 system Lot/code info: UDI 07350002010112
Official record: FDA (Device enforcement) ↗
Republished from the official source above; details can change — the source record controls.