The Medicines and Healthcare Products Regulatory Agency (MHRA), United Kingdom posted a field safety notice (FSN) concerning XVI R4.0 to R4.2.1, R4.5.0, R4.5.1 and R5.0.0 to R5.0.1, manufactured by Elekta.
Two different scenarios mentioned in the FSN can result from the same error. This issue may cause clinical mistreatment and collision risk resulting in fatal injury to the patient.
The manufacturer advises users of the followings:
A later software release of XVI will be supplied which gives a solution to this problem.
For details, please refer to MHRA website
http://www.mhra.gov.uk/Safetyinformation/Safetywarningsalertsandrecalls/fieldsafetynotices/CON433868
If you are in possession of the product, please contact your supplier for necessary actions.
Posted on 22 Jul 2014