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  • Dispositivo 374
  • Fabricante 58
  • Evento 124969
  • Implante 1
Alerta De Seguridad O Notificaciones De Seguridad para GLOBAL® UNITE® Platform Shoulder System
  • Tipo de evento
    Safety alert / Field Safety Notice
  • ID del evento
    2017/012/018/701/021
  • 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 Gynecare Thermachoice III catheter
  • Tipo de evento
    Safety alert / Field Safety Notice
  • ID del evento
    2015/012/003/291/006
  • Fecha de publicación del evento
    2015-12-02
  • 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 HARMONIC ACE® LAPAROSCOPIC 5MM DIAMETER SH...
  • Tipo de evento
    Safety alert / Field Safety Notice
  • ID del evento
    2018/005/004/478/021
  • 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 ILS Proximate Circular Stapler
  • Tipo de evento
    Safety alert / Field Safety Notice
  • ID del evento
    2019/003/028/701/016
  • Fecha de publicación del evento
    2019-03-29
  • 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 Impactor for PFNA Blade
  • Tipo de evento
    Safety alert / Field Safety Notice
  • ID del evento
    2016/012/012/291/031
  • Fecha de publicación del evento
    2017-04-21
  • 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 Impactor for PFNA Blade
  • Tipo de evento
    Safety alert / Field Safety Notice
  • ID del evento
    2016/012/012/291/031
  • 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 Inserter f/TEN
  • Tipo de evento
    Safety alert / Field Safety Notice
  • ID del evento
    2015/003/003/081/012
  • Fecha de publicación del evento
    2015-02-26
  • 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 Inserter f/TEN
  • Tipo de evento
    Safety alert / Field Safety Notice
  • ID del evento
    2015/003/003/081/012
  • Fecha de publicación del evento
    2015-07-15
  • 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 Insertion Handle for PFN
  • Tipo de evento
    Safety alert / Field Safety Notice
  • ID del evento
    2015/012/003/291/010
  • Fecha de publicación del evento
    2015-11-18
  • 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 LATARJET EXPERIENCE
  • Tipo de evento
    Safety alert / Field Safety Notice
  • ID del evento
    2017/005/023/291/027
  • Fecha de publicación del evento
    2017-05-18
  • 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 LATARJET EXPERIENCE Sharp Curved Osteotome
  • Tipo de evento
    Safety alert / Field Safety Notice
  • ID del evento
    2018/001/009/291/023
  • 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 LCP Drill Sleeve 1.5 f/Drill Bit ø1.1mm
  • Tipo de evento
    Safety alert / Field Safety Notice
  • ID del evento
    2017/008/014/071/001
  • Fecha de publicación del evento
    2017-08-07
  • 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 LCS COMPLETE RPS Knee System
  • Tipo de evento
    Safety alert / Field Safety Notice
  • ID del evento
    2015/003/009/121/010
  • 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 LINX Reflux Management System
  • Tipo de evento
    Safety alert / Field Safety Notice
  • ID del evento
    2018/004/024/291/015
  • Fecha de publicación del evento
    2018-04-13
  • 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 Matrix LOCK Screw ø1.85 self-tap L5 TAN, p...
  • Tipo de evento
    Safety alert / Field Safety Notice
  • ID del evento
    2017/006/023/291/014
  • Fecha de publicación del evento
    2017-06-21
  • 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 MegaPower Electrosurgical Generator
  • Tipo de evento
    Safety alert / Field Safety Notice
  • ID del evento
    2018/005/030/701/005
  • 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 MegaPower Electrosurgical Generator
  • Tipo de evento
    Safety alert / Field Safety Notice
  • ID del evento
    2018/005/030/701/005
  • 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 Neurovascular embolization coil Neurovascu...
  • Tipo de evento
    Safety alert / Field Safety Notice
  • ID del evento
    2017/002/002/299/006
  • Fecha de publicación del evento
    2017-01-31
  • 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 NMARQ circular irrigated catheter
  • Tipo de evento
    Safety alert / Field Safety Notice
  • ID del evento
    2015/006/022/291/017
  • Fecha de publicación del evento
    2015-06-24
  • 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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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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