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 Medtronic.

¿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 086 05 17 000
  • Fecha de inicio del evento
    2017-05-17
  • 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=11044
  • 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
    Manufacturer reinforces warning that device should be used only with medtronic instruments.

Device

NavLock Trackers Used with StealthStation Systems
  • Modelo / Serial
    Products: Part Nos.: Driver, Gray Assembly 9734228 Driver, Orange Assembly 9734259 Driver, Violet Assembly 9734315 Instrument Set NavLock 9734489 Instrument Set, Universal NavLock 9734833 NavLock Kit, Violet 9734837 NavLock Tracker Universal Green 9734734 NavLock Tracker Universal Grey 9734590 NavLock Tracker Universal Orange 9734683 NavLock Tracker Universal Violet 9734682 Tracker Kits, NavLock Universal Green 9734914 Tracker Kits, NavLock Universal Grey 9734906 Tracker Kits, NavLock Universal Orange 9734907 Tracker Kits, NavLock Universal Violet 9734908 NavLock TrackerTM and associated sets and kits: 9735120
  • Descripción del producto
    Stereotactic Systems, Image-Guided, Surgical, Intracranial
  • Manufacturer
    Medtronic

Manufacturer

Medtronic
  • Empresa matriz del fabricante (2017)
    Medtronic plc
  • Comentario del fabricante
    “If our surveillance systems identify a potential performance issue, our personnel promptly evaluate the problem, including, when appropriate, conducting root cause investigations and internal testing to assess whether the product continues to meet specifications and defined performance criteria,” Medtronic told ICIJ in a statement. “In some cases, based on this evaluation, Medtronic may determine that a recall is necessary.” The company said that it communicates with healthcare providers and/or patients and provide recommendations to address such issues. Medtronic noted that these communications can include letters, emails, calls, press releases, physician notifications and social media postings, as well as informing the FDA and other regulators of the actions.
  • Representante del fabricante
    Medtronic Saudi Arabia
  • Source
    SFDA