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  • Dispositivo 839
  • Fabricante 839
  • Evento 950
  • Implante 0
Retiro De Equipo (Recall) de THERA-TRAINER BALO and THERATRAINER VERTO
  • Tipo de evento
    Recall
  • ID del evento
    ARS/2018/14750
  • Fecha
    2018-10-02
  • País del evento
    Andorra
  • Fuente del evento
    HA
  • URL de la fuente del evento
    https://www.salut.ad/alertes/alertes.php?_pagi_pg=2&data1=&data2=&tipus=PRODUCTES%20SANITARIS%20-%20Retirada&titol=
  • Notas / Alertas
    Data from Andorra is current through November 2018. All of the data comes from Health Andorra, 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 Andorra.
  • Notas adicionales en la data
Retiro De Equipo (Recall) de IMMULITE/IMMULITE 1000
  • Tipo de evento
    Recall
  • ID del evento
    ARS/2017/11835
  • Fecha
    2017-01-02
  • País del evento
    Andorra
  • Fuente del evento
    HA
  • URL de la fuente del evento
    https://www.salut.ad/alertes/alertes.php?_pagi_pg=14&data1=&data2=&tipus=PRODUCTES%20DE%20DIAGN%D2STIC%20IN%20VITRO%20-%20Retirada&titol=
  • Notas / Alertas
    Data from Andorra is current through November 2018. All of the data comes from Health Andorra, 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 Andorra.
  • Notas adicionales en la data
Retiro De Equipo (Recall) de Vanguard Rocc, Vanguard Alpina, Alpina APS, Alpina APR, Alpina Uni, ...
  • Tipo de evento
    Recall
  • ID del evento
    ARS/2017/12343
  • Fecha
    2017-04-11
  • País del evento
    Andorra
  • Fuente del evento
    HA
  • URL de la fuente del evento
    https://www.salut.ad/alertes/alertes.php?_pagi_pg=38&data1=&data2=&tipus=PRODUCTES%20SANITARIS%20-%20Retirada&titol=
  • Notas / Alertas
    Data from Andorra is current through November 2018. All of the data comes from Health Andorra, 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 Andorra.
  • Notas adicionales en la data
Retiro De Equipo (Recall) de ROSA Brain
  • Tipo de evento
    Recall
  • ID del evento
    ARS/2017/12272
  • Fecha
    2017-03-29
  • País del evento
    Andorra
  • Fuente del evento
    HA
  • URL de la fuente del evento
    https://www.salut.ad/alertes/alertes.php?_pagi_pg=39&data1=&data2=&tipus=PRODUCTES%20SANITARIS%20-%20Retirada&titol=
  • Notas / Alertas
    Data from Andorra is current through November 2018. All of the data comes from Health Andorra, 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 Andorra.
  • Notas adicionales en la data
Retiro De Equipo (Recall) de Comprehensive Reverse Shoulder Prosthesis Tray
  • Tipo de evento
    Recall
  • ID del evento
    ARS/2017/12200
  • Fecha
    2017-03-13
  • País del evento
    Andorra
  • Fuente del evento
    HA
  • URL de la fuente del evento
    https://www.salut.ad/alertes/alertes.php?_pagi_pg=40&data1=&data2=&tipus=PRODUCTES%20SANITARIS%20-%20Retirada&titol=
  • Notas / Alertas
    Data from Andorra is current through November 2018. All of the data comes from Health Andorra, 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 Andorra.
  • Notas adicionales en la data
Retiro De Equipo (Recall) de Comprehensive Reverse Shoulder Prosthesis Tray
  • Tipo de evento
    Recall
  • ID del evento
    ARS/2017/11967
  • Fecha
    2017-01-30
  • País del evento
    Andorra
  • Fuente del evento
    HA
  • URL de la fuente del evento
    https://www.salut.ad/alertes/alertes.php?_pagi_pg=42&data1=&data2=&tipus=PRODUCTES%20SANITARIS%20-%20Retirada&titol=
  • Notas / Alertas
    Data from Andorra is current through November 2018. All of the data comes from Health Andorra, 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 Andorra.
  • Notas adicionales en la data
Retiro De Equipo (Recall) de CERTAIN implants
  • Tipo de evento
    Recall
  • ID del evento
    ARS/2017/11870
  • Fecha
    2017-01-13
  • País del evento
    Andorra
  • Fuente del evento
    HA
  • URL de la fuente del evento
    https://www.salut.ad/alertes/alertes.php?_pagi_pg=43&data1=&data2=&tipus=PRODUCTES%20SANITARIS%20-%20Retirada&titol=
  • Notas / Alertas
    Data from Andorra is current through November 2018. All of the data comes from Health Andorra, 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 Andorra.
  • Notas adicionales en la data
Retiro De Equipo (Recall) de RapidFlap SpinDown Clamp
  • Tipo de evento
    Recall
  • ID del evento
    ARS/2018/14868
  • Fecha
    2018-10-31
  • País del evento
    Andorra
  • Fuente del evento
    HA
  • URL de la fuente del evento
    https://www.salut.ad/alertes/alertes.php?_pagi_pg=1&data1=&data2=&tipus=PRODUCTES%20SANITARIS%20-%20Retirada&titol=
  • Notas / Alertas
    Data from Andorra is current through November 2018. All of the data comes from Health Andorra, 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 Andorra.
  • Notas adicionales en la data
Retiro De Equipo (Recall) de drill bit
  • Tipo de evento
    Recall
  • ID del evento
    ARS/2018/14634
  • Fecha
    2018-09-03
  • País del evento
    Andorra
  • Fuente del evento
    HA
  • URL de la fuente del evento
    https://www.salut.ad/alertes/alertes.php?_pagi_pg=4&data1=&data2=&tipus=PRODUCTES%20SANITARIS%20-%20Retirada&titol=
  • Notas / Alertas
    Data from Andorra is current through November 2018. All of the data comes from Health Andorra, 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 Andorra.
  • Notas adicionales en la data
Retiro De Equipo (Recall) de HIPLOC
  • Tipo de evento
    Recall
  • ID del evento
    ARS/2018/14609
  • Fecha
    2018-08-28
  • País del evento
    Andorra
  • Fuente del evento
    HA
  • URL de la fuente del evento
    https://www.salut.ad/alertes/alertes.php?_pagi_pg=4&data1=&data2=&tipus=PRODUCTES%20SANITARIS%20-%20Retirada&titol=
  • Notas / Alertas
    Data from Andorra is current through November 2018. All of the data comes from Health Andorra, 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 Andorra.
  • Notas adicionales en la data
Retiro De Equipo (Recall) de Affixus nail
  • Tipo de evento
    Recall
  • ID del evento
    ARS/2018/14608
  • Fecha
    2018-08-28
  • País del evento
    Andorra
  • Fuente del evento
    HA
  • URL de la fuente del evento
    https://www.salut.ad/alertes/alertes.php?_pagi_pg=4&data1=&data2=&tipus=PRODUCTES%20SANITARIS%20-%20Retirada&titol=
  • Notas / Alertas
    Data from Andorra is current through November 2018. All of the data comes from Health Andorra, 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 Andorra.
  • Notas adicionales en la data
Retiro De Equipo (Recall) de Stem set, Orthopedic Salvage System
  • Tipo de evento
    Recall
  • ID del evento
    ARS/2018/14060
  • Fecha
    2018-05-14
  • País del evento
    Andorra
  • Fuente del evento
    HA
  • URL de la fuente del evento
    https://www.salut.ad/alertes/alertes.php?_pagi_pg=11&data1=&data2=&tipus=PRODUCTES%20SANITARIS%20-%20Retirada&titol=
  • Notas / Alertas
    Data from Andorra is current through November 2018. All of the data comes from Health Andorra, 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 Andorra.
  • Notas adicionales en la data
Retiro De Equipo (Recall) de Avenir Muller stem
  • Tipo de evento
    Recall
  • ID del evento
    ARS/2018/13795
  • Fecha
    2018-03-20
  • País del evento
    Andorra
  • Fuente del evento
    HA
  • URL de la fuente del evento
    https://www.salut.ad/alertes/alertes.php?_pagi_pg=14&data1=&data2=&tipus=PRODUCTES%20SANITARIS%20-%20Retirada&titol=
  • Notas / Alertas
    Data from Andorra is current through November 2018. All of the data comes from Health Andorra, 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 Andorra.
  • Notas adicionales en la data
Retiro De Equipo (Recall) de Various hip and knee implants
  • Tipo de evento
    Recall
  • ID del evento
    ARS/2018/13544
  • Fecha
    2018-01-25
  • País del evento
    Andorra
  • Fuente del evento
    HA
  • URL de la fuente del evento
    https://www.salut.ad/alertes/alertes.php?_pagi_pg=18&data1=&data2=&tipus=PRODUCTES%20SANITARIS%20-%20Retirada&titol=
  • Notas / Alertas
    Data from Andorra is current through November 2018. All of the data comes from Health Andorra, 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 Andorra.
  • Notas adicionales en la data
Retiro De Equipo (Recall) de Implante MTX
  • Tipo de evento
    Recall
  • ID del evento
    ARS/2018/13503
  • Fecha
    2018-01-17
  • País del evento
    Andorra
  • Fuente del evento
    HA
  • URL de la fuente del evento
    https://www.salut.ad/alertes/alertes.php?_pagi_pg=19&data1=&data2=&tipus=PRODUCTES%20SANITARIS%20-%20Retirada&titol=
  • Notas / Alertas
    Data from Andorra is current through November 2018. All of the data comes from Health Andorra, 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 Andorra.
  • Notas adicionales en la data
Retiro De Equipo (Recall) de Implant Tapered Screw-Vent
  • Tipo de evento
    Recall
  • ID del evento
    ARS/2017/13338
  • Fecha
    2017-12-12
  • País del evento
    Andorra
  • Fuente del evento
    HA
  • URL de la fuente del evento
    https://www.salut.ad/alertes/alertes.php?_pagi_pg=21&data1=&data2=&tipus=PRODUCTES%20SANITARIS%20-%20Retirada&titol=
  • Notas / Alertas
    Data from Andorra is current through November 2018. All of the data comes from Health Andorra, 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 Andorra.
  • Notas adicionales en la data
Retiro De Equipo (Recall) de Implant Tapered Screw-Vent
  • Tipo de evento
    Recall
  • ID del evento
    ARS/2017/13339
  • Fecha
    2017-12-12
  • País del evento
    Andorra
  • Fuente del evento
    HA
  • URL de la fuente del evento
    https://www.salut.ad/alertes/alertes.php?_pagi_pg=21&data1=&data2=&tipus=PRODUCTES%20SANITARIS%20-%20Retirada&titol=
  • Notas / Alertas
    Data from Andorra is current through November 2018. All of the data comes from Health Andorra, 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 Andorra.
  • Notas adicionales en la data
Retiro De Equipo (Recall) de HexDriver with Gemlock
  • Tipo de evento
    Recall
  • ID del evento
    ARS/2017/13152
  • Fecha
    2017-10-27
  • País del evento
    Andorra
  • Fuente del evento
    HA
  • URL de la fuente del evento
    https://www.salut.ad/alertes/alertes.php?_pagi_pg=24&data1=&data2=&tipus=PRODUCTES%20SANITARIS%20-%20Retirada&titol=
  • Notas / Alertas
    Data from Andorra is current through November 2018. All of the data comes from Health Andorra, 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 Andorra.
  • Notas adicionales en la data
Retiro De Equipo (Recall) de Vanguard femoral components
  • Tipo de evento
    Recall
  • ID del evento
    ARS/2017/13098
  • Fecha
    2017-10-13
  • País del evento
    Andorra
  • Fuente del evento
    HA
  • URL de la fuente del evento
    https://www.salut.ad/alertes/alertes.php?_pagi_pg=25&data1=&data2=&tipus=PRODUCTES%20SANITARIS%20-%20Retirada&titol=
  • Notas / Alertas
    Data from Andorra is current through November 2018. All of the data comes from Health Andorra, 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 Andorra.
  • Notas adicionales en la data
Retiro De Equipo (Recall) de Vanguard femoral components
  • Tipo de evento
    Recall
  • ID del evento
    ARS/2017/13098
  • Fecha
    2017-10-13
  • País del evento
    Andorra
  • Fuente del evento
    HA
  • URL de la fuente del evento
    https://www.salut.ad/alertes/alertes.php?_pagi_pg=26&data1=&data2=&tipus=PRODUCTES%20SANITARIS%20-%20Retirada&titol=
  • Notas / Alertas
    Data from Andorra is current through November 2018. All of the data comes from Health Andorra, 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 Andorra.
  • Notas adicionales en la data
Retiro De Equipo (Recall) de Affixus nail
  • Tipo de evento
    Recall
  • ID del evento
    ARS/2017/13000
  • Fecha
    2017-09-19
  • País del evento
    Andorra
  • Fuente del evento
    HA
  • URL de la fuente del evento
    https://www.salut.ad/alertes/alertes.php?_pagi_pg=27&data1=&data2=&tipus=PRODUCTES%20SANITARIS%20-%20Retirada&titol=
  • Notas / Alertas
    Data from Andorra is current through November 2018. All of the data comes from Health Andorra, 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 Andorra.
  • Notas adicionales en la data
Retiro De Equipo (Recall) de Ziptight – Ti
  • Tipo de evento
    Recall
  • ID del evento
    ARS/2017/12977
  • Fecha
    2017-09-14
  • País del evento
    Andorra
  • Fuente del evento
    HA
  • URL de la fuente del evento
    https://www.salut.ad/alertes/alertes.php?_pagi_pg=28&data1=&data2=&tipus=PRODUCTES%20SANITARIS%20-%20Retirada&titol=
  • Notas / Alertas
    Data from Andorra is current through November 2018. All of the data comes from Health Andorra, 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 Andorra.
  • Notas adicionales en la data
Retiro De Equipo (Recall) de Persona impants
  • Tipo de evento
    Recall
  • ID del evento
    ARS/2017/12912
  • Fecha
    2017-08-25
  • País del evento
    Andorra
  • Fuente del evento
    HA
  • URL de la fuente del evento
    https://www.salut.ad/alertes/alertes.php?_pagi_pg=29&data1=&data2=&tipus=PRODUCTES%20SANITARIS%20-%20Retirada&titol=
  • Notas / Alertas
    Data from Andorra is current through November 2018. All of the data comes from Health Andorra, 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 Andorra.
  • Notas adicionales en la data
Retiro De Equipo (Recall) de Versys Beaded Hip Stem and Segmental Knee
  • Tipo de evento
    Recall
  • ID del evento
    ARS/2017/12899
  • Fecha
    2017-08-21
  • País del evento
    Andorra
  • Fuente del evento
    HA
  • URL de la fuente del evento
    https://www.salut.ad/alertes/alertes.php?_pagi_pg=29&data1=&data2=&tipus=PRODUCTES%20SANITARIS%20-%20Retirada&titol=
  • Notas / Alertas
    Data from Andorra is current through November 2018. All of the data comes from Health Andorra, 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 Andorra.
  • Notas adicionales en la data
Retiro De Equipo (Recall) de Various implants
  • Tipo de evento
    Recall
  • ID del evento
    ARS/2017/12234
  • Fecha
    2017-03-20
  • País del evento
    Andorra
  • Fuente del evento
    HA
  • URL de la fuente del evento
    https://www.salut.ad/alertes/alertes.php?_pagi_pg=39&data1=&data2=&tipus=PRODUCTES%20SANITARIS%20-%20Retirada&titol=
  • Notas / Alertas
    Data from Andorra is current through November 2018. All of the data comes from Health Andorra, 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 Andorra.
  • 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.