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Vista de la lista Vista de las tarjetas
  • Dispositivo 2
  • Fabricante 2
  • Evento 124969
  • Implante 0
Retiro De Equipo (Recall) de PointGuard anti stick fistula needle
  • Tipo de evento
    Recall
  • ID del evento
    2008-0381
  • Fecha
    2008-06-06
  • 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: M2
  • Causa
    Device failure / feature after commissioning - mechanical failure.
Retiro De Equipo (Recall) de Siesta MRI anaestesia workstation
  • Tipo de evento
    Recall
  • ID del evento
    2008-0383
  • Fecha
    2008-06-06
  • 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: MDV DK
  • Causa
    Device failure / feature before use - software.
Retiro De Equipo (Recall) de SPI Element Dental Implant, SPI Contact Dental Implant
  • Tipo de evento
    Recall
  • ID del evento
    2008-0387
  • Fecha
    2008-06-09
  • 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: MDV CH
  • Causa
    Device failure / feature before use - manufacturing.
Retiro De Equipo (Recall) de ADVIA Centaur HAV IgM
  • Tipo de evento
    Recall
  • ID del evento
    2008-0389
  • Fecha
    2008-06-10
  • 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: MDV IE
  • Causa
    Device failure / feature before use - software.
Retiro De Equipo (Recall) de NexStent Carotid Stent and Monorail Delivery System
  • Tipo de evento
    Recall
  • ID del evento
    2008-0395
  • Fecha
    2008-06-12
  • 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: M2
  • Causa
    Device failure / feature before use - manufacturing.
Retiro De Equipo (Recall) de ARROW CANNON CATHETER - CHRONIC HEMODIALYSIS CATHETER, ARROW CANNON ...
  • Tipo de evento
    Recall
  • ID del evento
    2008-0396
  • Fecha
    2008-06-13
  • 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: M2
  • Causa
    Device failure / feature after commissioning - mechanical failure.
Retiro De Equipo (Recall) de Gambro
  • Tipo de evento
    Recall
  • ID del evento
    2008-0401
  • Fecha
    2008-06-17
  • 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: MDV DE
  • Causa
    Device failure / feature before use - other.
Retiro De Equipo (Recall) de Access Immunoassay Ultrasensitive Insulin Reagent kit
  • Tipo de evento
    Recall
  • ID del evento
    2008-0402
  • Fecha
    2008-06-18
  • 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: MDV IE
  • Causa
    Device failure / feature before use - material / component.
Retiro De Equipo (Recall) de ADVIA Benzodiazapine Assay
  • Tipo de evento
    Recall
  • ID del evento
    2008-0424
  • Fecha
    2008-06-27
  • 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: MDV IE
  • Causa
    Device failure / feature before use - material / component.
Retiro De Equipo (Recall) de S/5 iCentral, Cardiovascular Monitoring Devices
  • Tipo de evento
    Recall
  • ID del evento
    2008-0425
  • Fecha
    2008-06-27
  • 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 US
  • Causa
    Device failure / feature before use - software.
Retiro De Equipo (Recall) de Portex Blue Line Ultra
  • Tipo de evento
    Recall
  • ID del evento
    2008-0427
  • Fecha
    2008-06-30
  • 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: M2
  • Causa
    Device failure / feature before use - labeling.
Retiro De Equipo (Recall) de Platinum Plus Coronary Guire Wire
  • Tipo de evento
    Recall
  • ID del evento
    2008-0428
  • Fecha
    2008-06-30
  • 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: M2
  • Causa
    Device failure / feature before use - manufacturing.
Retiro De Equipo (Recall) de Ortholock, Ortholock Ex Pins, Navigation Pins
  • Tipo de evento
    Recall
  • ID del evento
    2008-0429
  • Fecha
    2008-06-30
  • 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: M2
  • Causa
    Device failure / feature before use - packing - operating instructions.
Retiro De Equipo (Recall) de NexGen Complete Knee Solution MIS Total Knee Procedure Tibial Broach...
  • Tipo de evento
    Recall
  • ID del evento
    2008-0432
  • Fecha
    2008-07-01
  • 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: M2
  • Causa
    Device failure / feature before use - design.
Retiro De Equipo (Recall) de Tubing Pack
  • Tipo de evento
    Recall
  • ID del evento
    2008-0445
  • Fecha
    2008-07-04
  • 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: MDV DE
  • Causa
    Device failure / feature before use - manufacturing.
Retiro De Equipo (Recall) de Ascensia Contour, Contour TS
  • Tipo de evento
    Recall
  • ID del evento
    2008-0448
  • Fecha
    2008-07-08
  • 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: MDV CH, M2
  • Causa
    Device failure / feature before use - packing - operating instructions.
Retiro De Equipo (Recall) de C-Flex Endoureterotomy Stent Set
  • Tipo de evento
    Recall
  • ID del evento
    2008-0458
  • Fecha
    2008-07-17
  • 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: M2
  • Causa
    Device failure / feature before use - manufacturing.
Retiro De Equipo (Recall) de Difco Shigella Antiserum Poly Group B
  • Tipo de evento
    Recall
  • ID del evento
    2008-0475
  • Fecha
    2008-07-21
  • 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: MDV IE
  • Causa
    Device failure / feature before use - material / component.
Retiro De Equipo (Recall) de Pall Medical Arterial Blood Filter for Extracorporel Service (AL6B) ...
  • Tipo de evento
    Recall
  • ID del evento
    2008-0477
  • Fecha
    2008-07-22
  • 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: MDV UK
  • Causa
    Device failure / feature before use - manufacturing.
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