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Vista de la lista Vista de las tarjetas
  • Dispositivo 25
  • Fabricante 5
  • Evento 124969
  • Implante 0
Alerta De Seguridad O Notificaciones De Seguridad para Disposable Suction Kit
  • Tipo de evento
    Safety alert / Field Safety Notice
  • ID del evento
    2018/008/014/291/017
  • Fecha de publicación del evento
    2018-08-07
  • País del evento
    United Kingdom
  • Fuente del evento
    MHRA
  • Notas / Alertas
    Data from the United Kingdom is current through April 2019. All of the data comes from the Medicines and Healthcare products Regulatory Agency, 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 the United Kingdom.
  • Notas adicionales en la data
Alerta De Seguridad O Notificaciones De Seguridad para Temperature Probe General Purpose 9F
  • Tipo de evento
    Safety alert / Field Safety Notice
  • ID del evento
    2018/007/013/291/010
  • Fecha de publicación del evento
    2018-07-06
  • País del evento
    United Kingdom
  • Fuente del evento
    MHRA
  • Notas / Alertas
    Data from the United Kingdom is current through April 2019. All of the data comes from the Medicines and Healthcare products Regulatory Agency, 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 the United Kingdom.
  • Notas adicionales en la data
Alerta De Seguridad O Notificaciones De Seguridad para WATO EX-65, WATO EX-55, A5 and A7
  • Tipo de evento
    Safety alert / Field Safety Notice
  • ID del evento
    2017/007/003/291/036
  • País del evento
    United Kingdom
  • Fuente del evento
    MHRA
  • Notas / Alertas
    Data from the United Kingdom is current through April 2019. All of the data comes from the Medicines and Healthcare products Regulatory Agency, 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 the United Kingdom.
  • Notas adicionales en la data
Alerta De Seguridad O Notificaciones De Seguridad para Beneview T1 Patient Monitor
  • Tipo de evento
    Safety alert / Field Safety Notice
  • ID del evento
    2017/004/020/701/007
  • País del evento
    United Kingdom
  • Fuente del evento
    MHRA
  • Notas / Alertas
    Data from the United Kingdom is current through April 2019. All of the data comes from the Medicines and Healthcare products Regulatory Agency, 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 the United Kingdom.
  • Notas adicionales en la data
Alerta De Seguridad O Notificaciones De Seguridad para Dryline II Water Trap
  • Tipo de evento
    Safety alert / Field Safety Notice
  • ID del evento
    2016/008/030/291/023
  • País del evento
    United Kingdom
  • Fuente del evento
    MHRA
  • Notas / Alertas
    Data from the United Kingdom is current through April 2019. All of the data comes from the Medicines and Healthcare products Regulatory Agency, 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 the United Kingdom.
  • Notas adicionales en la data
Alerta De Seguridad O Notificaciones De Seguridad para BeneVision N22 and N19 patient monitors
  • Tipo de evento
    Safety alert / Field Safety Notice
  • ID del evento
    2016/007/004/701/020
  • País del evento
    United Kingdom
  • Fuente del evento
    MHRA
  • Notas / Alertas
    Data from the United Kingdom is current through April 2019. All of the data comes from the Medicines and Healthcare products Regulatory Agency, 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 the United Kingdom.
  • Notas adicionales en la data
Alerta De Seguridad O Notificaciones De Seguridad para FIXOL (Fixative for Kleihauer)
  • Tipo de evento
    Safety alert / Field Safety Notice
  • ID del evento
    2017/012/022/601/008
  • Fecha de publicación del evento
    2017-12-20
  • País del evento
    United Kingdom
  • Fuente del evento
    MHRA
  • Notas / Alertas
    Data from the United Kingdom is current through April 2019. All of the data comes from the Medicines and Healthcare products Regulatory Agency, 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 the United Kingdom.
  • Notas adicionales en la data
Alerta De Seguridad O Notificaciones De Seguridad para Fujifilm FDR Visionary Suite
  • Tipo de evento
    Safety alert / Field Safety Notice
  • ID del evento
    2017/006/013/701/009
  • País del evento
    United Kingdom
  • Fuente del evento
    MHRA
  • Notas / Alertas
    Data from the United Kingdom is current through April 2019. All of the data comes from the Medicines and Healthcare products Regulatory Agency, 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 the United Kingdom.
  • Notas adicionales en la data
Alerta De Seguridad O Notificaciones De Seguridad para RADspeed Series (Pro/CH-200/CH-200M)
  • Tipo de evento
    Safety alert / Field Safety Notice
  • ID del evento
    2017/006/029/701/007
  • Fecha de publicación del evento
    2017-05-26
  • País del evento
    United Kingdom
  • Fuente del evento
    MHRA
  • Notas / Alertas
    Data from the United Kingdom is current through April 2019. All of the data comes from the Medicines and Healthcare products Regulatory Agency, 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 the United Kingdom.
  • Notas adicionales en la data
Alerta De Seguridad O Notificaciones De Seguridad para Tissu-Trans
  • Tipo de evento
    Safety alert / Field Safety Notice
  • ID del evento
    2017/006/030/291/037
  • Fecha de publicación del evento
    2017-06-12
  • País del evento
    United Kingdom
  • Fuente del evento
    MHRA
  • Notas / Alertas
    Data from the United Kingdom is current through April 2019. All of the data comes from the Medicines and Healthcare products Regulatory Agency, 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 the United Kingdom.
  • Notas adicionales en la data
Alerta De Seguridad O Notificaciones De Seguridad para TissuTrans Filtron 100
  • Tipo de evento
    Safety alert / Field Safety Notice
  • ID del evento
    2018/003/007/478/005
  • Fecha de publicación del evento
    2018-01-10
  • País del evento
    United Kingdom
  • Fuente del evento
    MHRA
  • Notas / Alertas
    Data from the United Kingdom is current through April 2019. All of the data comes from the Medicines and Healthcare products Regulatory Agency, 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 the United Kingdom.
  • Notas adicionales en la data
Alerta De Seguridad O Notificaciones De Seguridad para Acuson NX2, NX2 Elite, NX3, NX3 Elite
  • Tipo de evento
    Safety alert / Field Safety Notice
  • ID del evento
    2019/002/005/601/006
  • País del evento
    United Kingdom
  • Fuente del evento
    MHRA
  • Notas / Alertas
    Data from the United Kingdom is current through April 2019. All of the data comes from the Medicines and Healthcare products Regulatory Agency, 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 the United Kingdom.
  • Notas adicionales en la data
Alerta De Seguridad O Notificaciones De Seguridad para ACUSON S family (S1000, S2000, S3000)
  • Tipo de evento
    Safety alert / Field Safety Notice
  • ID del evento
    2015/007/007/601/504
  • País del evento
    United Kingdom
  • Fuente del evento
    MHRA
  • Notas / Alertas
    Data from the United Kingdom is current through April 2019. All of the data comes from the Medicines and Healthcare products Regulatory Agency, 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 the United Kingdom.
  • Notas adicionales en la data
Alerta De Seguridad O Notificaciones De Seguridad para ACUSON S2000, S3000 with virtual touch IQ ...
  • Tipo de evento
    Safety alert / Field Safety Notice
  • ID del evento
    2015/007/007/601/505
  • País del evento
    United Kingdom
  • Fuente del evento
    MHRA
  • Notas / Alertas
    Data from the United Kingdom is current through April 2019. All of the data comes from the Medicines and Healthcare products Regulatory Agency, 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 the United Kingdom.
  • Notas adicionales en la data
Alerta De Seguridad O Notificaciones De Seguridad para Advia Centaur DHEAS, Advia Centaur CSA, Ad...
  • Tipo de evento
    Safety alert / Field Safety Notice
  • ID del evento
    2018/001/005/601/007
  • País del evento
    United Kingdom
  • Fuente del evento
    MHRA
  • Notas / Alertas
    Data from the United Kingdom is current through April 2019. All of the data comes from the Medicines and Healthcare products Regulatory Agency, 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 the United Kingdom.
  • Notas adicionales en la data
Alerta De Seguridad O Notificaciones De Seguridad para ADVIA Centaur Progesterone; Dimension Vist...
  • Tipo de evento
    Safety alert / Field Safety Notice
  • ID del evento
    2017/001/009/601/002
  • Fecha de publicación del evento
    2017-01-04
  • País del evento
    United Kingdom
  • Fuente del evento
    MHRA
  • Notas / Alertas
    Data from the United Kingdom is current through April 2019. All of the data comes from the Medicines and Healthcare products Regulatory Agency, 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 the United Kingdom.
  • Notas adicionales en la data
Alerta De Seguridad O Notificaciones De Seguridad para ADVIA Chemistry Assays, Dimension Assays, ...
  • Tipo de evento
    Safety alert / Field Safety Notice
  • ID del evento
    2017/007/013/601/003
  • País del evento
    United Kingdom
  • Fuente del evento
    MHRA
  • Notas / Alertas
    Data from the United Kingdom is current through April 2019. All of the data comes from the Medicines and Healthcare products Regulatory Agency, 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 the United Kingdom.
  • Notas adicionales en la data
Alerta De Seguridad O Notificaciones De Seguridad para Artis Q, Artis Q.zen
  • Tipo de evento
    Safety alert / Field Safety Notice
  • ID del evento
    2015/003/026/601/003
  • Fecha de publicación del evento
    2015-03-06
  • País del evento
    United Kingdom
  • Fuente del evento
    MHRA
  • Notas / Alertas
    Data from the United Kingdom is current through April 2019. All of the data comes from the Medicines and Healthcare products Regulatory Agency, 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 the United Kingdom.
  • Notas adicionales en la data
Alerta De Seguridad O Notificaciones De Seguridad para Artis systems with 19" Live Display
  • Tipo de evento
    Safety alert / Field Safety Notice
  • ID del evento
    2016/007/014/601/005
  • Fecha de publicación del evento
    2016-06-06
  • País del evento
    United Kingdom
  • Fuente del evento
    MHRA
  • Notas / Alertas
    Data from the United Kingdom is current through April 2019. All of the data comes from the Medicines and Healthcare products Regulatory Agency, 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 the United Kingdom.
  • Notas adicionales en la data
Alerta De Seguridad O Notificaciones De Seguridad para Artis zee Floor, Artis zee Biplane, Artis ...
  • Tipo de evento
    Safety alert / Field Safety Notice
  • ID del evento
    2015/005/027/601/001
  • Fecha de publicación del evento
    2015-05-19
  • País del evento
    United Kingdom
  • Fuente del evento
    MHRA
  • Notas / Alertas
    Data from the United Kingdom is current through April 2019. All of the data comes from the Medicines and Healthcare products Regulatory Agency, 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 the United Kingdom.
  • Notas adicionales en la data
Alerta De Seguridad O Notificaciones De Seguridad para Assembly group table of Ysio, Ysio Max and...
  • Tipo de evento
    Safety alert / Field Safety Notice
  • ID del evento
    2016/008/001/601/003
  • País del evento
    United Kingdom
  • Fuente del evento
    MHRA
  • Notas / Alertas
    Data from the United Kingdom is current through April 2019. All of the data comes from the Medicines and Healthcare products Regulatory Agency, 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 the United Kingdom.
  • Notas adicionales en la data
Alerta De Seguridad O Notificaciones De Seguridad para Business Area Advanced Therapies: Artis ze...
  • Tipo de evento
    Safety alert / Field Safety Notice
  • ID del evento
    2016/011/016/601/008
  • Fecha de publicación del evento
    2016-10-27
  • País del evento
    United Kingdom
  • Fuente del evento
    MHRA
  • Notas / Alertas
    Data from the United Kingdom is current through April 2019. All of the data comes from the Medicines and Healthcare products Regulatory Agency, 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 the United Kingdom.
  • Notas adicionales en la data
Alerta De Seguridad O Notificaciones De Seguridad para Dimension Gentamicin, Dimension Vista Gent...
  • Tipo de evento
    Safety alert / Field Safety Notice
  • ID del evento
    2018/004/025/601/010
  • País del evento
    United Kingdom
  • Fuente del evento
    MHRA
  • Notas / Alertas
    Data from the United Kingdom is current through April 2019. All of the data comes from the Medicines and Healthcare products Regulatory Agency, 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 the United Kingdom.
  • Notas adicionales en la data
Alerta De Seguridad O Notificaciones De Seguridad para Dimension TNI, DimnesioV DIGXN, E2, FERR, ...
  • Tipo de evento
    Safety alert / Field Safety Notice
  • ID del evento
    2017/004/003/601/004
  • País del evento
    United Kingdom
  • Fuente del evento
    MHRA
  • Notas / Alertas
    Data from the United Kingdom is current through April 2019. All of the data comes from the Medicines and Healthcare products Regulatory Agency, 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 the United Kingdom.
  • Notas adicionales en la data
Alerta De Seguridad O Notificaciones De Seguridad para Dimension® and Dimension Vista® AADVIA® Ch...
  • Tipo de evento
    Safety alert / Field Safety Notice
  • ID del evento
    2016/008/023/601/002
  • Fecha de publicación del evento
    2016-08-19
  • País del evento
    United Kingdom
  • Fuente del evento
    MHRA
  • Notas / Alertas
    Data from the United Kingdom is current through April 2019. All of the data comes from the Medicines and Healthcare products Regulatory Agency, 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 the United Kingdom.
  • Notas adicionales en la data
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Acerca de la base de datos

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Los dispositivos médicos ayudan con el diagnóstico, la prevención y el tratamiento de muchas lesiones y enfermedades. A través de la International Medical Devices Database no estamos sugiriendo que compañías u otras entidades mencionadas en la base de datos hayan sido parte de una conducta ilegal o hayan actuado de manera impropia. Un mismo dispositivo médico puede tener distintos nombres en diferentes países. Esta base de datos no busca proporcionar asesoría médica. Los pacientes deben consultar con sus médicos para determinar si la data contiene información relevante y si la misma tiene implicaciones médicas para ellos.

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