Retiro De Equipo (Recall) de Oncentra External Beam (formerly known as Oncentra MasterPlan during release of v3.x)(Radiation therapy treatment planning software)

Según Department of Health, Therapeutic Goods Administration, este evento ( retiro de equipo (recall) ) involucró a un dispositivo médico en Australia que fue producido por Nucletron Pty Limited.

¿Qué es esto?

Una corrección al equipo o acción de retiro tomada por el fabricante para abordar un problema con un dispositivo médico. Los retiros (recalls) ocurren cuando un dispositivo médico está defectuoso, cuando puede poner en riesgo la salud, o cuando simultáneamente está defectuoso y puede poner en riesgo la salud.

Más información acerca de la data acá
  • Tipo de evento
    Recall
  • ID del evento
    RC-2016-RN-01655-1
  • Clase de Riesgo del Evento
    Class II
  • Fecha de inicio del evento
    2016-12-22
  • País del evento
  • Fuente del evento
    DHTGA
  • URL de la fuente del evento
  • Notas / Alertas
    Australian data is current through July 2018. All of the data comes from the Australian Therapeutic Goods Administration, except for the categories Manufacturer Parent Company and Product Classification.
    The Parent Company and the Product Classification were added by ICIJ.
    The parent company information is based on 2017 public records. The device classification information comes from FDA’s Product Classification by Review Panel, based on matches of recall data from the U.S. and Australia.
  • Notas adicionales en la data
  • Causa
    If a physical wedge, for which the total field size limit perpendicular to the wedge direction is more than 10 cm larger than the field size limit in wedge direction, is inserted in in-plane direction (as seen with collimator angle 0 degrees), then with very large fields perpendicular to wedge direction a part of the scattered fluence can become unmodulated by the wedge. this will result in profile “horns” close to the edge of the field. the deviation is most prominent with the varian 60-degree wedge. the calculated overdose in the affected areas, towards the edges of the field, is typically 6% for clinically used field sizes locally. smaller deviations inside the field can also be observed with the varian 45-degree wedge. with all other inplane wedges, including the elekta motorised wedge, there is only an insignificant deformation of the cross profile tail, which is outside the treatment field.
  • Acción
    Elekta will be correcting the issue in the next upgrade of the Oncentra External Beam. In the interim, users are advised to not exceed jaw positions of +/- 12cm with the Varian 60-degree wedge and +/- 14.5 cm with the Varian 45-degree wedge in the direction perpendicular to the wedge slope, if the wedge is inserted in in-plane direction (collimator angle 0 degrees). In addition, Elekta is strongly advising users to perform proper Quality Assurance for all treatment plans before delivery of the first fraction to the patient.

Device

  • Modelo / Serial
    Oncentra External Beam (formerly known as Oncentra MasterPlan during release of v3.x)(Radiation therapy treatment planning software)All versionsARTG Number: 142110
  • Manufacturer

Manufacturer