Retiro De Equipo (Recall) de Brainlab Brain Metastases v1.0.0 and Adaptive Hybrid Surgery Analysis v1.0.0(Picture archiving and communication system (PACS) used in stereotactic, conformal, computer planned, Linac based radiation treatment of cranial, head and neck, and extracranial lesions)

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

¿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-2015-RN-01164-1
  • Clase de Riesgo del Evento
    Class I
  • Fecha de inicio del evento
    2015-11-27
  • 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
    Under very specific circumstances, there is the potential for large objects with fine resolution to be displayed cropped when imported from smartbrush into brainlab brain metastases1.0.0 or adaptive hybrid surgery analysis 1.0.0 for the brain metastases 1.0.0, if the cropped object is not recognised by the user before the plan is used for treatment and the deviation exceeds clinically acceptable limits, this could result in ineffective radiation treatment, serious patient injury, or even death of the patient. structures that are cropped in brain metastases are also cropped in the exported dicom rt structure set files. for the adaptive hybrid surgery analysis 1.0.0, if determination regarding the potential for radiotherapy is made, the incorrect information displayed can have an effect on clinical decisions. if the determination is done during surgery this could even, in a worst case scenario, mislead the user in regards to assessing the extent of resection during this surgery.
  • Acción
    Brainlab will provide a software update with this issue solved to affected customers. Brainlab will actively contact affected customers starting February 2016 to schedule the update. In the interim, users are advised to implement the following workarounds: After import always carefully review and verify all objects for correctness and validity. Always verify the correct shape of the objects in Brain Metastases or Adaptive Hybrid Surgery Analysis software. If possible do not use image data sets with large slice distance and/or with a low amount of slices. To retrospectively identify if cropped objects have been used for treatment planning, the object contours of a specific treatment plan can be reviewed in Brainlab Dose Review, where the error will also be visible. This action has been closed-out on 26/08/2016.

Device

  • Modelo / Serial
    Brainlab Brain Metastases v1.0.0 and Adaptive Hybrid Surgery Analysis v1.0.0(Picture archiving and communication system (PACS) used in stereotactic, conformal, computer planned, Linac based radiation treatment of cranial, head and neck, and extracranial lesions)ARTG Number: 230067
  • Manufacturer

Manufacturer