Medical device manufacturer, Elekta Limited, has issued a field safety notice concerning all XVI R4.5 systems.
Elekta recommended a mandatory software upgrade to all XVI R4.5 systems. The upgrade corrects the problem that prevents the operation of the database reindex function and prevents the error that incorrectly causes a kV gating inhibit during a segmental VolumeView™.
According to the local supplier, the affected system has been distributed in Hong Kong.
If you are in possession of the products, please contact your supplier for necessary actions.
Posted on 03 May 2012