• Acerca de la base de datos
  • ¿Cómo usar la IMDD?
  • Descargar la data
  • Preguntas frecuentes
  • Créditos
Vista de la lista Vista de las tarjetas
  • Dispositivo 55
  • Fabricante 55
  • Evento 63
  • Implante 0
Retiro De Equipo O Alerta De Seguridad para Patient monitor, Fetal monitor, B-Ultrasound Diagnosi...
  • Tipo de evento
    Recall / Safety alert
  • Fecha
    2013-06-27
  • País del evento
    Austria
  • Fuente del evento
    BASG
  • URL de la fuente del evento
    https://www.basg.gv.at/en/medical-devices/official-announcements/
  • Notas / Alertas
    Austrian data is current through September 2018. All of the data comes from the Austrian Federal Office for Safety in Health Care (BASG), 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 Austria.
  • Notas adicionales en la data
Retiro De Equipo O Alerta De Seguridad para Mini-Spacer with face mask
  • Tipo de evento
    Recall / Safety alert
  • Fecha
    2009-03-31
  • País del evento
    Austria
  • Fuente del evento
    BASG
  • URL de la fuente del evento
    https://www.basg.gv.at/en/medical-devices/official-announcements/
  • Notas / Alertas
    Austrian data is current through September 2018. All of the data comes from the Austrian Federal Office for Safety in Health Care (BASG), 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 Austria.
  • Notas adicionales en la data
Retiro De Equipo O Alerta De Seguridad para Skin Line Therapy
  • Tipo de evento
    Recall / Safety alert
  • Fecha
    2009-04-06
  • País del evento
    Austria
  • Fuente del evento
    BASG
  • URL de la fuente del evento
    https://www.basg.gv.at/en/medical-devices/official-announcements/
  • Notas / Alertas
    Austrian data is current through September 2018. All of the data comes from the Austrian Federal Office for Safety in Health Care (BASG), 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 Austria.
  • Notas adicionales en la data
Retiro De Equipo O Alerta De Seguridad para Hyacorp H1000 and Hyacorp HS
  • Tipo de evento
    Recall / Safety alert
  • Fecha
    2013-02-13
  • País del evento
    Austria
  • Fuente del evento
    BASG
  • URL de la fuente del evento
    https://www.basg.gv.at/en/medical-devices/official-announcements/
  • Notas / Alertas
    Austrian data is current through September 2018. All of the data comes from the Austrian Federal Office for Safety in Health Care (BASG), 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 Austria.
  • Notas adicionales en la data
Retiro De Equipo O Alerta De Seguridad para Intravascular catheter kits "ICY" for heat exchange, ...
  • Tipo de evento
    Recall / Safety alert
  • Fecha
    2013-05-28
  • País del evento
    Austria
  • Fuente del evento
    BASG
  • URL de la fuente del evento
    https://www.basg.gv.at/en/medical-devices/official-announcements/
  • Notas / Alertas
    Austrian data is current through September 2018. All of the data comes from the Austrian Federal Office for Safety in Health Care (BASG), 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 Austria.
  • Notas adicionales en la data
Retiro De Equipo O Alerta De Seguridad para PIP, M-Implants, Rofil Implant, TiBreeze
  • Tipo de evento
    Recall / Safety alert
  • Fecha
    2013-11-28
  • País del evento
    Austria
  • Fuente del evento
    BASG
  • URL de la fuente del evento
    https://www.basg.gv.at/en/medical-devices/official-announcements/
  • Notas / Alertas
    Austrian data is current through September 2018. All of the data comes from the Austrian Federal Office for Safety in Health Care (BASG), 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 Austria.
  • Notas adicionales en la data
Retiro De Equipo O Alerta De Seguridad para Anti HIV 1.2 Cassette, HBsAg Strip/Cassette Test, HCV...
  • Tipo de evento
    Recall / Safety alert
  • Fecha
    2013-11-07
  • País del evento
    Austria
  • Fuente del evento
    BASG
  • URL de la fuente del evento
    https://www.basg.gv.at/en/medical-devices/official-announcements/
  • Notas / Alertas
    Austrian data is current through September 2018. All of the data comes from the Austrian Federal Office for Safety in Health Care (BASG), 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 Austria.
  • Notas adicionales en la data
Retiro De Equipo O Alerta De Seguridad para Cereform breast implants and sizers
  • Tipo de evento
    Recall / Safety alert
  • Fecha
    2014-02-19
  • País del evento
    Austria
  • Fuente del evento
    BASG
  • URL de la fuente del evento
    https://www.basg.gv.at/en/medical-devices/official-announcements/
  • Notas / Alertas
    Austrian data is current through September 2018. All of the data comes from the Austrian Federal Office for Safety in Health Care (BASG), 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 Austria.
  • Notas adicionales en la data
Retiro De Equipo O Alerta De Seguridad para Testicular implant REF: PR3001, PR3002, PR3003, PR300...
  • Tipo de evento
    Recall / Safety alert
  • Fecha
    2015-10-15
  • País del evento
    Austria
  • Fuente del evento
    BASG
  • URL de la fuente del evento
    https://www.basg.gv.at/en/medical-devices/official-announcements/
  • Notas / Alertas
    Austrian data is current through September 2018. All of the data comes from the Austrian Federal Office for Safety in Health Care (BASG), 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 Austria.
  • Notas adicionales en la data
Retiro De Equipo O Alerta De Seguridad para ConMed Linvatech Hall Surgical Blades
  • Tipo de evento
    Recall / Safety alert
  • Fecha
    2008-03-20
  • País del evento
    Austria
  • Fuente del evento
    BASG
  • URL de la fuente del evento
    https://www.basg.gv.at/en/medical-devices/official-announcements/
  • Notas / Alertas
    Austrian data is current through September 2018. All of the data comes from the Austrian Federal Office for Safety in Health Care (BASG), 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 Austria.
  • Notas adicionales en la data
Retiro De Equipo O Alerta De Seguridad para Breastlight
  • Tipo de evento
    Recall / Safety alert
  • Fecha
    2012-09-21
  • País del evento
    Austria
  • Fuente del evento
    BASG
  • URL de la fuente del evento
    https://www.basg.gv.at/en/medical-devices/official-announcements/
  • Notas / Alertas
    Austrian data is current through September 2018. All of the data comes from the Austrian Federal Office for Safety in Health Care (BASG), 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 Austria.
  • Notas adicionales en la data
Retiro De Equipo O Alerta De Seguridad para Plain Catgut
  • Tipo de evento
    Recall / Safety alert
  • Fecha
    2008-10-17
  • País del evento
    Austria
  • Fuente del evento
    BASG
  • URL de la fuente del evento
    https://www.basg.gv.at/en/medical-devices/official-announcements/
  • Notas / Alertas
    Austrian data is current through September 2018. All of the data comes from the Austrian Federal Office for Safety in Health Care (BASG), 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 Austria.
  • Notas adicionales en la data
Retiro De Equipo O Alerta De Seguridad para Respisense Ditto, Respisense Data
  • Tipo de evento
    Recall / Safety alert
  • Fecha
    2015-07-02
  • País del evento
    Austria
  • Fuente del evento
    BASG
  • URL de la fuente del evento
    https://www.basg.gv.at/en/medical-devices/official-announcements/
  • Notas / Alertas
    Austrian data is current through September 2018. All of the data comes from the Austrian Federal Office for Safety in Health Care (BASG), 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 Austria.
  • Notas adicionales en la data
Retiro De Equipo O Alerta De Seguridad para da Vinci Surgical Systems
  • Tipo de evento
    Recall / Safety alert
  • Fecha
    2012-07-02
  • País del evento
    Austria
  • Fuente del evento
    BASG
  • URL de la fuente del evento
    https://www.basg.gv.at/en/medical-devices/official-announcements/
  • Notas / Alertas
    Austrian data is current through September 2018. All of the data comes from the Austrian Federal Office for Safety in Health Care (BASG), 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 Austria.
  • Notas adicionales en la data
Retiro De Equipo O Alerta De Seguridad para JUVÉDERM ULTRA 4
  • Tipo de evento
    Recall / Safety alert
  • Fecha
    2014-12-22
  • País del evento
    Austria
  • Fuente del evento
    BASG
  • URL de la fuente del evento
    https://www.basg.gv.at/en/medical-devices/official-announcements/
  • Notas / Alertas
    Austrian data is current through September 2018. All of the data comes from the Austrian Federal Office for Safety in Health Care (BASG), 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 Austria.
  • Notas adicionales en la data
Retiro De Equipo O Alerta De Seguridad para Aquilon2, Aquilon, Aquilon+ and Aquilon Pro series ne...
  • Tipo de evento
    Recall / Safety alert
  • Fecha
    2018-07-18
  • País del evento
    Austria
  • Fuente del evento
    BASG
  • URL de la fuente del evento
    https://www.basg.gv.at/en/medical-devices/official-announcements/
  • Notas / Alertas
    Austrian data is current through September 2018. All of the data comes from the Austrian Federal Office for Safety in Health Care (BASG), 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 Austria.
  • Notas adicionales en la data
Retiro De Equipo O Alerta De Seguridad para ArgoGuide Hydrophilic Wires
  • Tipo de evento
    Recall / Safety alert
  • Fecha
    2008-01-25
  • País del evento
    Austria
  • Fuente del evento
    BASG
  • URL de la fuente del evento
    https://www.basg.gv.at/en/medical-devices/official-announcements/
  • Notas / Alertas
    Austrian data is current through September 2018. All of the data comes from the Austrian Federal Office for Safety in Health Care (BASG), 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 Austria.
  • Notas adicionales en la data
Retiro De Equipo O Alerta De Seguridad para DePuy ASR and ASR XL
  • Tipo de evento
    Recall / Safety alert
  • Fecha
    2010-09-08
  • País del evento
    Austria
  • Fuente del evento
    BASG
  • URL de la fuente del evento
    https://www.basg.gv.at/en/medical-devices/official-announcements/
  • Notas / Alertas
    Austrian data is current through September 2018. All of the data comes from the Austrian Federal Office for Safety in Health Care (BASG), 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 Austria.
  • Notas adicionales en la data
Retiro De Equipo O Alerta De Seguridad para Cristal Face
  • Tipo de evento
    Recall / Safety alert
  • Fecha
    2012-01-19
  • País del evento
    Austria
  • Fuente del evento
    BASG
  • URL de la fuente del evento
    https://www.basg.gv.at/en/medical-devices/official-announcements/
  • Notas / Alertas
    Austrian data is current through September 2018. All of the data comes from the Austrian Federal Office for Safety in Health Care (BASG), 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 Austria.
  • Notas adicionales en la data
Retiro De Equipo O Alerta De Seguridad para MITCH TRH (total hip endoprosthesis system)
  • Tipo de evento
    Recall / Safety alert
  • Fecha
    2012-05-29
  • País del evento
    Austria
  • Fuente del evento
    BASG
  • URL de la fuente del evento
    https://www.basg.gv.at/en/medical-devices/official-announcements/
  • Notas / Alertas
    Austrian data is current through September 2018. All of the data comes from the Austrian Federal Office for Safety in Health Care (BASG), 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 Austria.
  • Notas adicionales en la data
Retiro De Equipo O Alerta De Seguridad para Tibreeze
  • Tipo de evento
    Recall / Safety alert
  • Fecha
    2012-02-07
  • País del evento
    Austria
  • Fuente del evento
    BASG
  • URL de la fuente del evento
    https://www.basg.gv.at/en/medical-devices/official-announcements/
  • Notas / Alertas
    Austrian data is current through September 2018. All of the data comes from the Austrian Federal Office for Safety in Health Care (BASG), 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 Austria.
  • Notas adicionales en la data
Retiro De Equipo O Alerta De Seguridad para Samaritan PAD 500P
  • Tipo de evento
    Recall / Safety alert
  • Fecha
    2015-03-11
  • País del evento
    Austria
  • Fuente del evento
    BASG
  • URL de la fuente del evento
    https://www.basg.gv.at/en/medical-devices/official-announcements/
  • Notas / Alertas
    Austrian data is current through September 2018. All of the data comes from the Austrian Federal Office for Safety in Health Care (BASG), 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 Austria.
  • Notas adicionales en la data
Retiro De Equipo O Alerta De Seguridad para Heartware 1400, 1401XX, 1407XX, 1408
  • Tipo de evento
    Recall / Safety alert
  • Fecha
    2013-06-11
  • País del evento
    Austria
  • Fuente del evento
    BASG
  • URL de la fuente del evento
    https://www.basg.gv.at/en/medical-devices/official-announcements/
  • Notas / Alertas
    Austrian data is current through September 2018. All of the data comes from the Austrian Federal Office for Safety in Health Care (BASG), 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 Austria.
  • Notas adicionales en la data
  • Causa
    The manufacturer, heartware inc., in this safety information document, warns you about the urgent need to observe the operating instructions when operating and maintaining heartware heart support systems.
Retiro De Equipo O Alerta De Seguridad para Sterilization envelopes, autosealable, disposable
  • Tipo de evento
    Recall / Safety alert
  • Fecha
    2014-11-18
  • País del evento
    Austria
  • Fuente del evento
    BASG
  • URL de la fuente del evento
    https://www.basg.gv.at/en/medical-devices/official-announcements/
  • Notas / Alertas
    Austrian data is current through September 2018. All of the data comes from the Austrian Federal Office for Safety in Health Care (BASG), 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 Austria.
  • Notas adicionales en la data
Retiro De Equipo O Alerta De Seguridad para GemStar™ Infusion System, Plum A+/A+ 3 Family of Infu...
  • Tipo de evento
    Recall / Safety alert
  • Fecha
    2013-03-18
  • País del evento
    Austria
  • Fuente del evento
    BASG
  • URL de la fuente del evento
    https://www.basg.gv.at/en/medical-devices/official-announcements/
  • Notas / Alertas
    Austrian data is current through September 2018. All of the data comes from the Austrian Federal Office for Safety in Health Care (BASG), 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 Austria.
  • Notas adicionales en la data
  • 1
  • 2
  • 3
  • Next ›
  • Last »

Acerca de la base de datos

Explore más de 120,000 registros de retiros, alertas y notificaciones de seguridad de dispositivos médicos y sus conexiones con los fabricantes.

  • Preguntas frecuentes
  • Acerca de la base de datos
  • Contáctenos
  • Créditos

Historias en su correo

¿Trabaja en la industria médica? ¿O tiene experiencia con algún dispositivo médico? Nuestra reportería no ha terminado. Queremos oír de usted.

¡Cuéntanos tu historia!

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.