RayStation/RayPlan 8B, Build Number 8.1.0.47, stand-alone software treatment planning system
Check against the official notice below — it lists the full affected range.
RaySearch Laboratories AB is recalling RayStation/RayPlan version 8B, Build Number 8.1.0.47, a stand-alone software treatment planning system. The recalled system has a defect where erroneous tabletop position information may be propagated when pitch or roll correction is applied. Although pitch and roll correction itself is not propagated, any non-zero pitch or roll values cause the lateral, longitudinal, and vertical position values that are propagated to be incorrect.
One system was distributed in the United States, specifically to Tennessee. The recalled system has the UDI 07350002010129. The recall record does not specify what actions affected consumers should take.
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 in the U.S. Lot/code info: UDI 07350002010129
Official record: FDA (Device enforcement) ↗
Republished from the official source above; details can change — the source record controls.