Events

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 Radiometer Medical.

¿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 159 09 12 000
  • Fecha de inicio del evento
    2012-09-25
  • País del evento
    Saudi Arabia
  • Fuente del evento
    SFDA
  • URL de la fuente del evento
    https://ncmdr.sfda.gov.sa/Secure/CA/CaViewRecall.aspx?caid=4&rid=2414
  • 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
    The root cause for the carry-over has been identified to be a deficiency in some cup wash units. that is, the steel tube, which empties the cup during the cup wash process, is too long causing it to touch the bottom of the cup. in this situation an un-bound tracer-analyte complex can bind to the tube and carry-over into subsequent tests. the countermeasure, which reduces the length of the steel tube by 0.4mm to ensure that there is a clearance between the tube and the bottom of the cup.

Device

analyzers, AQT90 FLEX
  • Modelo / Serial
    AQT90 FLEX: 393-838R0143N0001 Cup wash unit: 903-119 (shipped as of October 31)
  • Descripción del producto
    IVD, analyzers
  • Manufacturer
    Radiometer Medical

Manufacturer

Radiometer Medical
  • Empresa matriz del fabricante (2017)
    Danaher Corporation
  • Representante del fabricante
    Salehiya Trading Est., Riyadh, (01) 2628939
  • Source
    SFDA