Alerta De Seguridad para Brain Metastases v1.0.0 and Adaptive Hybrid Surgery Analysis v1.0.0

Según Department of Health, este evento ( alerta de seguridad ) involucró a un dispositivo médico en Hong Kong que fue producido por Brainlab.

¿Qué es esto?

Las alertas proporcionan información importante y recomendaciones sobre los productos. Aunque se haya emitido una alerta, esto no significa necesariamente que el producto se considera peligroso. Las alertas de seguridad, dirigidas a trabajadores de la salud y a usuarios, pueden incluir retiro de equipos. Pueden ser escritas por los fabricantes, pero también por funcionarios del área de salud.

Más información acerca de la data acá
  • Tipo de evento
    Safety alert
  • Fecha
    2015-12-01
  • Fecha de publicación del evento
    2015-12-01
  • País del evento
  • Fuente del evento
    DH
  • URL de la fuente del evento
  • Notas / Alertas
    Hong Kong data is current through September 2018. All of the data comes from the Department of Health (Hong Kong), 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 data from the U.S. and Hong Kong.
  • Notas adicionales en la data
    Medical Device Safety Alert
  • Causa
    Medical device safety alert: brainlab brain metastases v1.0.0 and adaptive hybrid surgery analysis v1.0.0 the therapeutic goods administration (tga) of australia has posted a medical device safety alert concerning the brainlab brain metastases v1.0.0 and adaptive hybrid surgery analysis v1.0.0 manufactured by brainlab. 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 metastases v1.0.0 or adaptive hybrid surgery analysis v1.0.0. for the brain metastases v1.0.0, 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 v1.0.0, 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. the manufacturer will provide a software update with this issue solved. in the interim, users are advised to implement the workarounds instruction provided by the manufacturer. for details, please refer to the tga website:http://apps.Tga.Gov.Au/prod/sara/arn-detail.Aspx?k=rc-2015-rn-01164-1 if you are in possession of the affected products, please contact your supplier for necessary actions. posted on 1 december 2015.

Device

  • Modelo / Serial
  • Descripción del producto
    Medical Device Safety Alert: Brainlab Brain Metastases v1.0.0 and Adaptive Hybrid Surgery Analysis v1.0.0
  • Manufacturer

Manufacturer