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 040 11 12 001
  • Fecha de inicio del evento
    2014-01-30
  • 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=5208
  • 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
    Radiometer recently became aware that some membranes may have enzyme residues on the outer membrane. upon replacement of the lactate membrane the enzyme residue may cause an initial negative bias on the reported lactate result. the bias decreases over the in-use time, and depending on the amount of residue it may take anything between hours and days for the bias to disappear. worst case the bias upon membrane replacement is -1.5 mmol/l at lactate levels over 7.0 mmol/l. this is most apparent when comparing results measured before and immediately after membrane replacement.

Device

Lactate membrane units
  • Modelo / Serial
    The membrane units affected are: All lots of 942-066 When used on:ABL700 Series, and ABL800 Analyzers.
  • Descripción del producto
    measuring, Lactate, membrane, 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