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Vista de la lista Vista de las tarjetas
  • Dispositivo 183
  • Fabricante 87
  • Evento 124969
  • Implante 15
Notificaciones De Seguridad De Campo acerca de Sex Hormone Binding Globulin (SHBG) IVD
  • Tipo de evento
    Field Safety Notice
  • ID del evento
    Vk_20170213_08
  • Fecha de publicación del evento
    2017-02-20
  • País del evento
    Switzerland
  • Fuente del evento
    SATP
  • URL de la fuente del evento
    https://fsca.swissmedic.ch/mep/#?q=Vk_20170213_08
  • Notas / Alertas
    The data from Switzerland is current through March 2018. All of the data comes from Swiss Agency for Therapeutic Products, 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 Switzerland.
  • Notas adicionales en la data
Notificaciones De Seguridad De Campo acerca de IMMULITE®/IMMULITE® 1000/IMMULITE® 2000/IMMULITE® ...
  • Tipo de evento
    Field Safety Notice
  • ID del evento
    Vk_20171221_07
  • Fecha de publicación del evento
    2017-12-27
  • Estado del evento
    2017-12-27
  • País del evento
    Switzerland
  • Fuente del evento
    SATP
  • URL de la fuente del evento
    https://fsca.swissmedic.ch/mep/#?q=Vk_20171221_07
  • Notas / Alertas
    The data from Switzerland is current through March 2018. All of the data comes from Swiss Agency for Therapeutic Products, 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 Switzerland.
  • Notas adicionales en la data
Notificaciones De Seguridad De Campo acerca de Immulite ACHT Control Module
  • Tipo de evento
    Field Safety Notice
  • ID del evento
    Vk_20121010_07
  • Fecha de publicación del evento
    2012-10-15
  • País del evento
    Switzerland
  • Fuente del evento
    SATP
  • URL de la fuente del evento
    https://fsca.swissmedic.ch/mep/#?q=Vk_20121010_07
  • Notas / Alertas
    The data from Switzerland is current through March 2018. All of the data comes from Swiss Agency for Therapeutic Products, 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 Switzerland.
  • Notas adicionales en la data
Notificaciones De Seguridad De Campo acerca de IMMULITE
  • Tipo de evento
    Field Safety Notice
  • ID del evento
    Vk_20130710_07
  • Fecha de publicación del evento
    2013-07-15
  • País del evento
    Switzerland
  • Fuente del evento
    SATP
  • URL de la fuente del evento
    https://fsca.swissmedic.ch/mep/#?q=Vk_20130710_07
  • Notas / Alertas
    The data from Switzerland is current through March 2018. All of the data comes from Swiss Agency for Therapeutic Products, 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 Switzerland.
  • Notas adicionales en la data
Notificaciones De Seguridad De Campo acerca de IMMULITE 1000
  • Tipo de evento
    Field Safety Notice
  • ID del evento
    Vk_20130710_07
  • Fecha de publicación del evento
    2013-07-15
  • País del evento
    Switzerland
  • Fuente del evento
    SATP
  • URL de la fuente del evento
    https://fsca.swissmedic.ch/mep/#?q=Vk_20130710_07
  • Notas / Alertas
    The data from Switzerland is current through March 2018. All of the data comes from Swiss Agency for Therapeutic Products, 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 Switzerland.
  • Notas adicionales en la data
Notificaciones De Seguridad De Campo acerca de IMMULITE 2000
  • Tipo de evento
    Field Safety Notice
  • ID del evento
    Vk_20130710_07
  • Fecha de publicación del evento
    2013-07-15
  • País del evento
    Switzerland
  • Fuente del evento
    SATP
  • URL de la fuente del evento
    https://fsca.swissmedic.ch/mep/#?q=Vk_20130710_07
  • Notas / Alertas
    The data from Switzerland is current through March 2018. All of the data comes from Swiss Agency for Therapeutic Products, 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 Switzerland.
  • Notas adicionales en la data
Notificaciones De Seguridad De Campo acerca de IMMULITE 2000 Xpi
  • Tipo de evento
    Field Safety Notice
  • ID del evento
    Vk_20130710_07
  • Fecha de publicación del evento
    2013-07-15
  • País del evento
    Switzerland
  • Fuente del evento
    SATP
  • URL de la fuente del evento
    https://fsca.swissmedic.ch/mep/#?q=Vk_20130710_07
  • Notas / Alertas
    The data from Switzerland is current through March 2018. All of the data comes from Swiss Agency for Therapeutic Products, 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 Switzerland.
  • Notas adicionales en la data
Notificaciones De Seguridad De Campo acerca de Artis system with 19 inch live display
  • Tipo de evento
    Field Safety Notice
  • ID del evento
    Vk_20160725_09
  • Fecha de publicación del evento
    2016-08-02
  • País del evento
    Switzerland
  • Fuente del evento
    SATP
  • URL de la fuente del evento
    https://fsca.swissmedic.ch/mep/#?q=Vk_20160725_09
  • Notas / Alertas
    The data from Switzerland is current through March 2018. All of the data comes from Swiss Agency for Therapeutic Products, 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 Switzerland.
  • Notas adicionales en la data
Notificaciones De Seguridad De Campo acerca de AXIOM Artis; Artis zee; Artis Q/Q zen
  • Tipo de evento
    Field Safety Notice
  • ID del evento
    Vk_20160802_12
  • Fecha de publicación del evento
    2016-08-16
  • País del evento
    Switzerland
  • Fuente del evento
    SATP
  • URL de la fuente del evento
    https://fsca.swissmedic.ch/mep/#?q=Vk_20160802_12
  • Notas / Alertas
    The data from Switzerland is current through March 2018. All of the data comes from Swiss Agency for Therapeutic Products, 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 Switzerland.
  • Notas adicionales en la data
Notificaciones De Seguridad De Campo acerca de Artis Zee
  • Tipo de evento
    Field Safety Notice
  • ID del evento
    Vk_20161123_06
  • Fecha de publicación del evento
    2016-12-05
  • País del evento
    Switzerland
  • Fuente del evento
    SATP
  • URL de la fuente del evento
    https://fsca.swissmedic.ch/mep/#?q=Vk_20161123_06
  • Notas / Alertas
    The data from Switzerland is current through March 2018. All of the data comes from Swiss Agency for Therapeutic Products, 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 Switzerland.
  • Notas adicionales en la data
Notificaciones De Seguridad De Campo acerca de Mammomat Inspiration-System
  • Tipo de evento
    Field Safety Notice
  • ID del evento
    Vk_20170112_11
  • Fecha de publicación del evento
    2017-01-23
  • País del evento
    Switzerland
  • Fuente del evento
    SATP
  • URL de la fuente del evento
    https://fsca.swissmedic.ch/mep/#?q=Vk_20170112_11
  • Notas / Alertas
    The data from Switzerland is current through March 2018. All of the data comes from Swiss Agency for Therapeutic Products, 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 Switzerland.
  • Notas adicionales en la data
Notificaciones De Seguridad De Campo acerca de AXIOM Artis systems
  • Tipo de evento
    Field Safety Notice
  • ID del evento
    Vk_20170220_14
  • Fecha de publicación del evento
    2017-03-06
  • País del evento
    Switzerland
  • Fuente del evento
    SATP
  • URL de la fuente del evento
    https://fsca.swissmedic.ch/mep/#?q=Vk_20170220_14
  • Notas / Alertas
    The data from Switzerland is current through March 2018. All of the data comes from Swiss Agency for Therapeutic Products, 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 Switzerland.
  • Notas adicionales en la data
Notificaciones De Seguridad De Campo acerca de Artis system with wireless foot switch
  • Tipo de evento
    Field Safety Notice
  • ID del evento
    Vk_20170320_06
  • Fecha de publicación del evento
    2017-03-27
  • País del evento
    Switzerland
  • Fuente del evento
    SATP
  • URL de la fuente del evento
    https://fsca.swissmedic.ch/mep/#?q=Vk_20170320_06
  • Notas / Alertas
    The data from Switzerland is current through March 2018. All of the data comes from Swiss Agency for Therapeutic Products, 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 Switzerland.
  • Notas adicionales en la data
Notificaciones De Seguridad De Campo acerca de Artis Systems
  • Tipo de evento
    Field Safety Notice
  • ID del evento
    Vk_20170626_05
  • Fecha de publicación del evento
    2017-07-10
  • País del evento
    Switzerland
  • Fuente del evento
    SATP
  • URL de la fuente del evento
    https://fsca.swissmedic.ch/mep/#?q=Vk_20170626_05
  • Notas / Alertas
    The data from Switzerland is current through March 2018. All of the data comes from Swiss Agency for Therapeutic Products, 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 Switzerland.
  • Notas adicionales en la data
Notificaciones De Seguridad De Campo acerca de Artis system with wireless foot switch
  • Tipo de evento
    Field Safety Notice
  • ID del evento
    Vk_20171002_08
  • Fecha de publicación del evento
    2017-10-09
  • País del evento
    Switzerland
  • Fuente del evento
    SATP
  • URL de la fuente del evento
    https://fsca.swissmedic.ch/mep/#?q=Vk_20171002_08
  • Notas / Alertas
    The data from Switzerland is current through March 2018. All of the data comes from Swiss Agency for Therapeutic Products, 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 Switzerland.
  • Notas adicionales en la data
Notificaciones De Seguridad De Campo acerca de SOMATOM Definition
  • Tipo de evento
    Field Safety Notice
  • ID del evento
    Vk_20171108_09
  • Fecha de publicación del evento
    2017-11-14
  • País del evento
    Switzerland
  • Fuente del evento
    SATP
  • URL de la fuente del evento
    https://fsca.swissmedic.ch/mep/#?q=Vk_20171108_09
  • Notas / Alertas
    The data from Switzerland is current through March 2018. All of the data comes from Swiss Agency for Therapeutic Products, 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 Switzerland.
  • Notas adicionales en la data
Notificaciones De Seguridad De Campo acerca de SOMATOM Definition
  • Tipo de evento
    Field Safety Notice
  • ID del evento
    Vk_20171123_04
  • Fecha de publicación del evento
    2017-11-29
  • Estado del evento
    2017-11-29
  • País del evento
    Switzerland
  • Fuente del evento
    SATP
  • URL de la fuente del evento
    https://fsca.swissmedic.ch/mep/#?q=Vk_20171123_04
  • Notas / Alertas
    The data from Switzerland is current through March 2018. All of the data comes from Swiss Agency for Therapeutic Products, 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 Switzerland.
  • Notas adicionales en la data
Notificaciones De Seguridad De Campo acerca de SOMATOM FORCE
  • Tipo de evento
    Field Safety Notice
  • ID del evento
    Vk_20171123_04
  • Fecha de publicación del evento
    2017-11-29
  • Estado del evento
    2017-11-29
  • País del evento
    Switzerland
  • Fuente del evento
    SATP
  • URL de la fuente del evento
    https://fsca.swissmedic.ch/mep/#?q=Vk_20171123_04
  • Notas / Alertas
    The data from Switzerland is current through March 2018. All of the data comes from Swiss Agency for Therapeutic Products, 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 Switzerland.
  • Notas adicionales en la data
Notificaciones De Seguridad De Campo acerca de SOMATOM GO.UP and SOMATOM go.Now
  • Tipo de evento
    Field Safety Notice
  • ID del evento
    Vk_20180103_14
  • Fecha de publicación del evento
    2018-01-04
  • Estado del evento
    2018-01-04
  • País del evento
    Switzerland
  • Fuente del evento
    SATP
  • URL de la fuente del evento
    https://fsca.swissmedic.ch/mep/#?q=Vk_20180103_14
  • Notas / Alertas
    The data from Switzerland is current through March 2018. All of the data comes from Swiss Agency for Therapeutic Products, 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 Switzerland.
  • Notas adicionales en la data
Notificaciones De Seguridad De Campo acerca de SOMATOM
  • Tipo de evento
    Field Safety Notice
  • ID del evento
    Vk_20180226_07
  • Fecha de publicación del evento
    2018-02-28
  • Estado del evento
    2018-02-28
  • País del evento
    Switzerland
  • Fuente del evento
    SATP
  • URL de la fuente del evento
    https://fsca.swissmedic.ch/mep/#?q=Vk_20180226_07
  • Notas / Alertas
    The data from Switzerland is current through March 2018. All of the data comes from Swiss Agency for Therapeutic Products, 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 Switzerland.
  • Notas adicionales en la data
Notificaciones De Seguridad De Campo acerca de AXIOM Artis systems
  • Tipo de evento
    Field Safety Notice
  • ID del evento
    Vk_20161128_05
  • Fecha de publicación del evento
    2016-12-05
  • País del evento
    Switzerland
  • Fuente del evento
    SATP
  • URL de la fuente del evento
    https://fsca.swissmedic.ch/mep/#?q=Vk_20161128_05
  • Notas / Alertas
    The data from Switzerland is current through March 2018. All of the data comes from Swiss Agency for Therapeutic Products, 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 Switzerland.
  • Notas adicionales en la data
Notificaciones De Seguridad De Campo acerca de AXIOM Artis; Artis zee; Artis Q/Q zen
  • Tipo de evento
    Field Safety Notice
  • ID del evento
    Vk_20161219_06
  • Fecha de publicación del evento
    2017-01-09
  • Estado del evento
    2017-01-09
  • País del evento
    Switzerland
  • Fuente del evento
    SATP
  • URL de la fuente del evento
    https://fsca.swissmedic.ch/mep/#?q=Vk_20161219_06
  • Notas / Alertas
    The data from Switzerland is current through March 2018. All of the data comes from Swiss Agency for Therapeutic Products, 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 Switzerland.
  • Notas adicionales en la data
Notificaciones De Seguridad De Campo acerca de Artis Q/Q.zen
  • Tipo de evento
    Field Safety Notice
  • ID del evento
    Vk_20170308_11
  • Fecha de publicación del evento
    2017-03-20
  • País del evento
    Switzerland
  • Fuente del evento
    SATP
  • URL de la fuente del evento
    https://fsca.swissmedic.ch/mep/#?q=Vk_20170308_11
  • Notas / Alertas
    The data from Switzerland is current through March 2018. All of the data comes from Swiss Agency for Therapeutic Products, 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 Switzerland.
  • Notas adicionales en la data
Notificaciones De Seguridad De Campo acerca de Sensis System
  • Tipo de evento
    Field Safety Notice
  • ID del evento
    Vk_20170503_05
  • Fecha de publicación del evento
    2017-07-18
  • Estado del evento
    2017-07-18
  • País del evento
    Switzerland
  • Fuente del evento
    SATP
  • URL de la fuente del evento
    https://fsca.swissmedic.ch/mep/#?q=Vk_20170503_05
  • Notas / Alertas
    The data from Switzerland is current through March 2018. All of the data comes from Swiss Agency for Therapeutic Products, 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 Switzerland.
  • Notas adicionales en la data
Notificaciones De Seguridad De Campo acerca de Arcadis
  • Tipo de evento
    Field Safety Notice
  • ID del evento
    Vk_20170704_04
  • Fecha de publicación del evento
    2017-07-18
  • País del evento
    Switzerland
  • Fuente del evento
    SATP
  • URL de la fuente del evento
    https://fsca.swissmedic.ch/mep/#?q=Vk_20170704_04
  • Notas / Alertas
    The data from Switzerland is current through March 2018. All of the data comes from Swiss Agency for Therapeutic Products, 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 Switzerland.
  • Notas adicionales en la data
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