ELEKTA INC
VERSA HD · General Hospital
Recalls (5)
Due to a manufacturing issue and electrical grounding of systems.
Elekta has identified that if the microswitch within the middle arm is incorrectly setup, there is a potential for an uncontrolled extension of iViewGT / XVI detector arms. When the detector arm is fully deployed there is no risk of uncontrolled extension.
A component within a limited number of Elekta Linacs has been realized to be non-compliant to IEC 60601
There is a risk that the Diode D1 in the Modulator can fail in a destructive manner when removed from the machine, and that the protective tube surrounding the diode may fail to contain the ejected matter.
There is a potential for an uncontrolled extension of iViewGT / XVI detector arms.
FDA Classification (66)
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