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Vista de la lista Vista de las tarjetas
  • Dispositivo 193
  • Fabricante 46
  • Evento 124969
  • Implante 11
Retiro De Equipo (Recall) de AQT90 FLEX Analyzer
  • Tipo de evento
    Recall
  • ID del evento
    2010-0405
  • Fecha
    2010-04-30
  • País del evento
    Finland
  • Fuente del evento
    VNSAWH
  • Notas / Alertas
    Finnish data is current through April 2018. All of the data comes from Valvira - National Supervisory Authority for Welfare and Health, 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 Finland.
  • Notas adicionales en la data
    Source: FSCA
  • Causa
    Device failure / feature before use - software.
Retiro De Equipo (Recall) de 5.5 mm TroQSL Trocar
  • Tipo de evento
    Recall
  • ID del evento
    2010-0406
  • Fecha
    2010-04-30
  • País del evento
    Finland
  • Fuente del evento
    VNSAWH
  • Notas / Alertas
    Finnish data is current through April 2018. All of the data comes from Valvira - National Supervisory Authority for Welfare and Health, 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 Finland.
  • Notas adicionales en la data
    Source: FSCA
  • Causa
    Device failure / feature before use - manufacturing.
Retiro De Equipo (Recall) de 5008 & 5008S
  • Tipo de evento
    Recall
  • ID del evento
    2010-0408
  • Fecha
    2010-04-30
  • País del evento
    Finland
  • Fuente del evento
    VNSAWH
  • Notas / Alertas
    Finnish data is current through April 2018. All of the data comes from Valvira - National Supervisory Authority for Welfare and Health, 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 Finland.
  • Notas adicionales en la data
    Source: NCAR
  • Causa
    Device failure / feature before use - material / component.
Retiro De Equipo (Recall) de Inion CPS Biodegradable Fixation System, Inion CPS Baby Biodegradabl...
  • Tipo de evento
    Recall
  • ID del evento
    2010-0409
  • Fecha
    2010-04-30
  • País del evento
    Finland
  • Fuente del evento
    VNSAWH
  • Notas / Alertas
    Finnish data is current through April 2018. All of the data comes from Valvira - National Supervisory Authority for Welfare and Health, 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 Finland.
  • Notas adicionales en la data
    Source: FSCA
  • Causa
    Device failure / feature before use - instructions.
Retiro De Equipo (Recall) de Sinustamponaden / Sinus Packing
  • Tipo de evento
    Recall
  • ID del evento
    2010-0410
  • Fecha
    2010-05-04
  • País del evento
    Finland
  • Fuente del evento
    VNSAWH
  • Notas / Alertas
    Finnish data is current through April 2018. All of the data comes from Valvira - National Supervisory Authority for Welfare and Health, 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 Finland.
  • Notas adicionales en la data
    Source: NCAR
  • Causa
    Device failure / feature before use - manufacturing.
Retiro De Equipo (Recall) de PK7200 Blood Grouping System
  • Tipo de evento
    Recall
  • ID del evento
    2010-0411
  • Fecha
    2010-05-04
  • País del evento
    Finland
  • Fuente del evento
    VNSAWH
  • Notas / Alertas
    Finnish data is current through April 2018. All of the data comes from Valvira - National Supervisory Authority for Welfare and Health, 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 Finland.
  • Notas adicionales en la data
    Source: NCAR
  • Causa
    Device failure / feature before use - software.
Retiro De Equipo (Recall) de NexGen  Complete Knee Solution Stemmed Tibial Broach Impactor
  • Tipo de evento
    Recall
  • ID del evento
    2010-0412
  • Fecha
    2010-05-04
  • País del evento
    Finland
  • Fuente del evento
    VNSAWH
  • Notas / Alertas
    Finnish data is current through April 2018. All of the data comes from Valvira - National Supervisory Authority for Welfare and Health, 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 Finland.
  • Notas adicionales en la data
    Source: FSCA
  • Causa
    Device failure / feature before use - material / component.
Retiro De Equipo (Recall) de AQT90 FLEX Analyzer, Catalog No. 393-838
  • Tipo de evento
    Recall
  • ID del evento
    2010-0415
  • Fecha
    2010-05-04
  • País del evento
    Finland
  • Fuente del evento
    VNSAWH
  • Notas / Alertas
    Finnish data is current through April 2018. All of the data comes from Valvira - National Supervisory Authority for Welfare and Health, 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 Finland.
  • Notas adicionales en la data
    Source: NCAR
  • Causa
    Device failure / feature before use - software.
Retiro De Equipo (Recall) de Ulnar Shortening saw Blade – Hub Style S
  • Tipo de evento
    Recall
  • ID del evento
    2010-0416
  • Fecha
    2010-05-04
  • País del evento
    Finland
  • Fuente del evento
    VNSAWH
  • Notas / Alertas
    Finnish data is current through April 2018. All of the data comes from Valvira - National Supervisory Authority for Welfare and Health, 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 Finland.
  • Notas adicionales en la data
    Source: FSCA
  • Causa
    Device failure / feature before use - manufacturing.
Retiro De Equipo (Recall) de Access® Immunoassay Systems Estradiol
  • Tipo de evento
    Recall
  • ID del evento
    2010-0417
  • Fecha
    2010-05-04
  • País del evento
    Finland
  • Fuente del evento
    VNSAWH
  • Notas / Alertas
    Finnish data is current through April 2018. All of the data comes from Valvira - National Supervisory Authority for Welfare and Health, 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 Finland.
  • Notas adicionales en la data
    Source: NCAR
  • Causa
    Device failure / feature before use - material / component.
Retiro De Equipo (Recall) de UniCel® DxC 600, UniCel® DxC 600 PRO, UniCel® DxC 600i, UniCel® DxC ...
  • Tipo de evento
    Recall
  • ID del evento
    2010-0419
  • Fecha
    2010-05-04
  • País del evento
    Finland
  • Fuente del evento
    VNSAWH
  • Notas / Alertas
    Finnish data is current through April 2018. All of the data comes from Valvira - National Supervisory Authority for Welfare and Health, 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 Finland.
  • Notas adicionales en la data
    Source: NCAR
  • Causa
    Device failure / feature before use - packing - operating instructions.
Retiro De Equipo (Recall) de VariSource iX version 1.1
  • Tipo de evento
    Recall
  • ID del evento
    2010-0424
  • Fecha
    2010-05-05
  • País del evento
    Finland
  • Fuente del evento
    VNSAWH
  • Notas / Alertas
    Finnish data is current through April 2018. All of the data comes from Valvira - National Supervisory Authority for Welfare and Health, 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 Finland.
  • Notas adicionales en la data
    Source: FSCA
  • Causa
    Device failure / feature before use - software.
Retiro De Equipo (Recall) de STA Cephascreen 4
  • Tipo de evento
    Recall
  • ID del evento
    2010-0432
  • Fecha
    2010-05-05
  • País del evento
    Finland
  • Fuente del evento
    VNSAWH
  • Notas / Alertas
    Finnish data is current through April 2018. All of the data comes from Valvira - National Supervisory Authority for Welfare and Health, 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 Finland.
  • Notas adicionales en la data
    Source: FSCA
  • Causa
    Device failure / feature before use - manufacturing.
Retiro De Equipo (Recall) de Back-up Meier Steerable Guidewire
  • Tipo de evento
    Recall
  • ID del evento
    2010-0438
  • Fecha
    2010-05-06
  • País del evento
    Finland
  • Fuente del evento
    VNSAWH
  • Notas / Alertas
    Finnish data is current through April 2018. All of the data comes from Valvira - National Supervisory Authority for Welfare and Health, 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 Finland.
  • Notas adicionales en la data
    Source: FSCA
  • Causa
    Device failure / feature before use - manufacturing.
Retiro De Equipo (Recall) de FastPlan Treatment Planning System
  • Tipo de evento
    Recall
  • ID del evento
    2010-0439
  • Fecha
    2010-05-06
  • País del evento
    Finland
  • Fuente del evento
    VNSAWH
  • Notas / Alertas
    Finnish data is current through April 2018. All of the data comes from Valvira - National Supervisory Authority for Welfare and Health, 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 Finland.
  • Notas adicionales en la data
    Source: NCAR
  • Causa
    Operating error.
Retiro De Equipo (Recall) de Symbiq
  • Tipo de evento
    Recall
  • ID del evento
    2010-0440
  • Fecha
    2010-05-06
  • País del evento
    Finland
  • Fuente del evento
    VNSAWH
  • Notas / Alertas
    Finnish data is current through April 2018. All of the data comes from Valvira - National Supervisory Authority for Welfare and Health, 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 Finland.
    ICU Medical, Inc. acquired from Pfizer in early 2017, Hospira Infusion Systems, the portion of Hospira dedicated to develop infusion pumps.
  • Notas adicionales en la data
    Source: NCAR
  • Causa
    Device failure / feature before use - software.
Retiro De Equipo (Recall) de BHR Stream Introducer
  • Tipo de evento
    Recall
  • ID del evento
    2010-0455
  • Fecha
    2010-05-10
  • País del evento
    Finland
  • Fuente del evento
    VNSAWH
  • Notas / Alertas
    Finnish data is current through April 2018. All of the data comes from Valvira - National Supervisory Authority for Welfare and Health, 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 Finland.
  • Notas adicionales en la data
    Source: NCAR
  • Causa
    Device failure / feature before use - design.
Retiro De Equipo (Recall) de Peri-Loc Screw
  • Tipo de evento
    Recall
  • ID del evento
    2010-0459
  • Fecha
    2010-05-11
  • País del evento
    Finland
  • Fuente del evento
    VNSAWH
  • Notas / Alertas
    Finnish data is current through April 2018. All of the data comes from Valvira - National Supervisory Authority for Welfare and Health, 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 Finland.
  • Notas adicionales en la data
    Source: FSCA
  • Causa
    Device failure / feature before use - packing - sterility.
Retiro De Equipo (Recall) de Aneroid Sphygmomanometers Stethoscope
  • Tipo de evento
    Recall
  • ID del evento
    2010-0462
  • Fecha
    2010-05-11
  • País del evento
    Finland
  • Fuente del evento
    VNSAWH
  • Notas / Alertas
    Finnish data is current through April 2018. All of the data comes from Valvira - National Supervisory Authority for Welfare and Health, 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 Finland.
  • Notas adicionales en la data
    Source: NCAR
  • Causa
    Device failure / feature before use - packing - labeling.
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