translation missing: es.activerecord.attributes.event.titles.recall_field_safety_notice

Según Saudi Food & Drug Authority, este evento ( translation missing: es.activerecord.attributes.event.types.recall_field_safety_notice ) involucró a un dispositivo médico en Saudi Arabia que fue producido por Philips Healthcare.

¿Qué es esto?

Las notificaciones de seguridad de campo son comunicaciones sobre acciones que se pueden estar tomando en relación con un producto que se encuentra en el mercado, enviadas por los fabricantes de dispositivos médicos o sus representantes. Estas notificaciones son principalmente para trabajadores de la salud, pero también para usuarios. Pueden incluir alertas y retiro de equipos.

Más información acerca de la data acá
  • Tipo de evento
    Recall / Field Safety Notice
  • ID del evento
    mdprc 010 07 14 000
  • Fecha de inicio del evento
    2014-07-02
  • País del evento
  • Fuente del evento
    SFDA
  • URL de la fuente del evento
  • Notas / Alertas
    Saudi data is current through January 2019. All of the data comes from the Saudi Food & Drug Authority, 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 Saudi Arabia.
  • Notas adicionales en la data
    Report Source: NCMDR
    SFDA urges all hospitals that have devices subjected to recall, to contact the company.
  • Causa
    Philips received a report from the field that the fpd failed to remain securely locked in the deployed position. during a daily xct quality assurance phantom scan for image quality and hounsfield unit (hu) linearity an operator experienced resistance when engaging the locking handle of the fpd in the deployed position. with the locking handle in the locked position, the fpd locking mechanism was not locked, moved unexpectedly and contacted the imaging detector during system movement. philips’ investigation determined the internal linkage shaft broke preventing the fpd from being locked into its correct deployed position.

Device

  • Modelo / Serial
    - BrightView XCT - BrightView X- upgraded with the XCT Flat Panel Detector (FPD)
  • Descripción del producto
    SPECT/CT System
  • Manufacturer

Manufacturer

  • Empresa matriz del fabricante (2017)
  • Representante del fabricante
    Al-Faisaliah Medical System, Riyadh, (01) 2119948
  • Source
    SFDA