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  • Dispositivo 29
  • Fabricante 16
  • Evento 124969
  • Implante 0
Alerta De Seguridad O Notificaciones De Seguridad para LFIT Anatomic CoCr V40 Femoral Heads
  • Tipo de evento
    Safety alert / Field Safety Notice
  • ID del evento
    2016/009/028/701/006
  • Fecha de publicación del evento
    2017-03-13
  • 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 LFIT Anatomic CoCr V40 Femoral Heads
  • Tipo de evento
    Safety alert / Field Safety Notice
  • ID del evento
    2018/005/025/291/022
  • 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 LFIT Anatomic CoCr V40 Femoral Heads
  • Tipo de evento
    Safety alert / Field Safety Notice
  • ID del evento
    2018/011/013/291/008
  • Fecha de publicación del evento
    2018-10-18
  • 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 LFIT Anatomic CoCr V40 Femoral Heads
  • Tipo de evento
    Safety alert / Field Safety Notice
  • ID del evento
    2016/009/028/701/006
  • 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 LIFEPAK 1000 AEDs
  • Tipo de evento
    Safety alert / Field Safety Notice
  • ID del evento
    2017/001/019/291/001
  • 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 LIFEPAK 1000 defibrillator
  • Tipo de evento
    Safety alert / Field Safety Notice
  • ID del evento
    2015/008/026/291/002
  • 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 Lifepak 15 monitor/defibrillator
  • Tipo de evento
    Safety alert / Field Safety Notice
  • ID del evento
    2015/003/016/401/015
  • 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 LIFEPAK 15 monitor/defibrillator
  • Tipo de evento
    Safety alert / Field Safety Notice
  • ID del evento
    2019/002/004/291/012
  • Fecha de publicación del evento
    2019-02-06
  • 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 LIFEPAK CR Plus AED and LIFEPAK EXPRESS AED
  • Tipo de evento
    Safety alert / Field Safety Notice
  • ID del evento
    2016/008/003/299/011
  • 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 LIFEPAK EXPRESS® AED, LIFEPAK CR® Plus AED...
  • Tipo de evento
    Safety alert / Field Safety Notice
  • ID del evento
    2017/012/014/228/011
  • 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 LIFEPAK® 15 MONITOR/DEFIBRILLATOR
  • Tipo de evento
    Safety alert / Field Safety Notice
  • ID del evento
    2017/007/019/701/015
  • 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 LIFEPAK® 20e defibrillator/monitor
  • Tipo de evento
    Safety alert / Field Safety Notice
  • ID del evento
    2018/002/009/701/015
  • 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 MAKO
  • Tipo de evento
    Safety alert / Field Safety Notice
  • ID del evento
    2018/007/030/228/013
  • 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 MAKO RIO Spare Part Ethernet-Fiber Optic C...
  • Tipo de evento
    Safety alert / Field Safety Notice
  • ID del evento
    2018/001/025/701/013
  • 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 MCK TIBIAL BASEPLATE-RM/LL-SZ 2 & 7
  • Tipo de evento
    Safety alert / Field Safety Notice
  • ID del evento
    2017/012/020/291/001
  • 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 METS Femoral Plateau Plate
  • Tipo de evento
    Safety alert / Field Safety Notice
  • ID del evento
    2016/006/001/291/015
  • Fecha de publicación del evento
    2016-05-31
  • 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 METS Modular Proximal Humerus System
  • Tipo de evento
    Safety alert / Field Safety Notice
  • ID del evento
    2016/012/021/291/007
  • Fecha de publicación del evento
    2016-12-20
  • 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 METS modular proximal tibial replacement
  • Tipo de evento
    Safety alert / Field Safety Notice
  • ID del evento
    2015/001/007/081/024
  • Fecha de publicación del evento
    2015-01-23
  • 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 METS Modular Tumour System
  • Tipo de evento
    Safety alert / Field Safety Notice
  • ID del evento
    2016/011/024/701/019
  • Fecha de publicación del evento
    2016-11-25
  • 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 METS Principal Shaft
  • Tipo de evento
    Safety alert / Field Safety Notice
  • ID del evento
    2017/010/030/291/003
  • Fecha de publicación del evento
    2017-10-26
  • 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 MIS (Minimally Invasive Surgery) Toolsteel...
  • Tipo de evento
    Safety alert / Field Safety Notice
  • ID del evento
    2016/012/012/701/010
  • 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 MIS Distal Captures
  • Tipo de evento
    Safety alert / Field Safety Notice
  • ID del evento
    2015/010/015/292/001
  • 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 Navigation System II-Cart
  • Tipo de evento
    Safety alert / Field Safety Notice
  • ID del evento
    2015/006/015/291/022
  • Fecha de publicación del evento
    2015-05-18
  • 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 Neptune 2 Docking Station – Actuator Assembly
  • Tipo de evento
    Safety alert / Field Safety Notice
  • ID del evento
    2015/008/019/291/002
  • Fecha de publicación del evento
    2015-08-25
  • 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 Offset Cup Reamer Handle
  • Tipo de evento
    Safety alert / Field Safety Notice
  • ID del evento
    2016/011/004/291/006
  • Fecha de publicación del evento
    2016-10-17
  • 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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Aviso

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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