Alerta De Seguridad para iPlan RT Dose version 4.1

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

¿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
    2012-06-22
  • Fecha de publicación del evento
    2012-06-22
  • 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 iplan rt dose version 4.1 medical device manufacturer, brainlab ag issued a medical device safety alert concerning radiation therapy treatment planning system iplan rt dose version 4.1 (v. 4.1.0, 4.1.1 and 4.1.2). according to brainlab, iplan rt dose 4.1 might position the isocenters and rt structures in the dicom ct image files incorrectly if all of the following conditions are met: two or more ct image sets have the same “frame of reference” (same coordinate system). the selected “reference set” and “alignment set” in iplan rt are different ct image sets, but have the same “frame of reference”. for the “reference set” and “alignment set” the used scanner settings differed at least in one of the following parameters: - pixel size - scan range (number of ct images and position) - slice thickness/distance or - matrix size the dicom “full export” - this is not the default “r& v export” - is used to export to a non-brainlab system (e.G. to another radiation therapy treatment planning system). brainlab explained that if all of the conditions above are met, the treatment dose might be delivered to a region different from the planned one. if the deviation would exceed clinically acceptable limits and at the same time be small enough to remain undetected, this could result in serious patient injury and/or ineffective treatment. according to the local supplier, the affected products have been distributed in hong kong. if you are in possession of the affected products, please contact your supplier for necessary actions. posted on 22 june 2012.

Device

  • Modelo / Serial
  • Descripción del producto
    Medical Device Safety Alert: Brainlab iPlan RT Dose version 4.1
  • Manufacturer

Manufacturer