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  • Dispositivo 11
  • Fabricante 8
  • Evento 124969
  • Implante 0
Retiro De Equipo (Recall) de MENINGOCOCCUS AGGLUTINATING SERA GROUP: ABCDKXYZW135
  • Tipo de evento
    Recall
  • ID del evento
    41278
  • Clase de Riesgo del Evento
    III
  • Fecha de inicio del evento
    1996-04-10
  • País del evento
    Canada
  • Fuente del evento
    HC
  • Notas / Alertas
    Canadian data is current through March 2018. All of the data comes from Health Canada, 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 Canada.
  • Notas adicionales en la data
Retiro De Equipo (Recall) de MEDI-MAN ELECTRIC PATIENT LIFT
  • Tipo de evento
    Recall
  • ID del evento
    27733
  • Clase de Riesgo del Evento
    III
  • Fecha de inicio del evento
    1996-04-12
  • País del evento
    Canada
  • Fuente del evento
    HC
  • Notas / Alertas
    Canadian data is current through March 2018. All of the data comes from Health Canada, 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 Canada.
  • Notas adicionales en la data
Retiro De Equipo (Recall) de LIT HOPITAL (ELECTRIQUE) BERTEC
  • Tipo de evento
    Recall
  • ID del evento
    34747
  • Clase de Riesgo del Evento
    II
  • Fecha de inicio del evento
    1996-04-15
  • País del evento
    Canada
  • Fuente del evento
    HC
  • Notas / Alertas
    Canadian data is current through March 2018. All of the data comes from Health Canada, 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 Canada.
  • Notas adicionales en la data
Retiro De Equipo (Recall) de BBL SEPTI-CHEK SLIDE
  • Tipo de evento
    Recall
  • ID del evento
    88705
  • Clase de Riesgo del Evento
    III
  • Fecha de inicio del evento
    1996-04-16
  • País del evento
    Canada
  • Fuente del evento
    HC
  • Notas / Alertas
    Canadian data is current through March 2018. All of the data comes from Health Canada, 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 Canada.
  • Notas adicionales en la data
Retiro De Equipo (Recall) de BACTEC MYCO/F-SPUTA CULTURE VIALS
  • Tipo de evento
    Recall
  • ID del evento
    42680
  • Clase de Riesgo del Evento
    III
  • Fecha de inicio del evento
    1996-04-16
  • País del evento
    Canada
  • Fuente del evento
    HC
  • Notas / Alertas
    Canadian data is current through March 2018. All of the data comes from Health Canada, 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 Canada.
  • Notas adicionales en la data
Retiro De Equipo (Recall) de BBL MGIT (MYCOBACTERIA GROWTH INDICATOR TUBE) PANTA
  • Tipo de evento
    Recall
  • ID del evento
    27335
  • Clase de Riesgo del Evento
    III
  • Fecha de inicio del evento
    1996-04-16
  • País del evento
    Canada
  • Fuente del evento
    HC
  • Notas / Alertas
    Canadian data is current through March 2018. All of the data comes from Health Canada, 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 Canada.
  • Notas adicionales en la data
Retiro De Equipo (Recall) de KODAK SURECELL CHLAMYDIA TEST KIT
  • Tipo de evento
    Recall
  • ID del evento
    47104
  • Clase de Riesgo del Evento
    III
  • Fecha de inicio del evento
    1996-04-17
  • País del evento
    Canada
  • Fuente del evento
    HC
  • Notas / Alertas
    Canadian data is current through March 2018. All of the data comes from Health Canada, 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 Canada.
  • Notas adicionales en la data
Retiro De Equipo (Recall) de SYNCHRON CX5 SYSTEM ANALYZER - CLASS 2
  • Tipo de evento
    Recall
  • ID del evento
    15902
  • Clase de Riesgo del Evento
    II
  • Fecha de inicio del evento
    1996-04-18
  • País del evento
    Canada
  • Fuente del evento
    HC
  • Notas / Alertas
    Canadian data is current through March 2018. All of the data comes from Health Canada, 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 Canada.
  • Notas adicionales en la data
Retiro De Equipo (Recall) de MICRO-JEWEL ACTIVE CAN ELECTRODE ARRHYTHMIA MANAGEMENT DEVICE
  • Tipo de evento
    Recall
  • ID del evento
    86280
  • Clase de Riesgo del Evento
    II
  • Fecha de inicio del evento
    1996-04-23
  • País del evento
    Canada
  • Fuente del evento
    HC
  • Notas / Alertas
    Canadian data is current through March 2018. All of the data comes from Health Canada, 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 Canada.
  • Notas adicionales en la data
Retiro De Equipo (Recall) de HDI 3000 ULTRASOUND SYSTEM
  • Tipo de evento
    Recall
  • ID del evento
    42891
  • Clase de Riesgo del Evento
    II
  • Fecha de inicio del evento
    1996-04-23
  • País del evento
    Canada
  • Fuente del evento
    HC
  • Notas / Alertas
    Canadian data is current through March 2018. All of the data comes from Health Canada, 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 Canada.
  • Notas adicionales en la data
Retiro De Equipo (Recall) de FIRST MEDIC 710 SEMI-AUTOMATIC DEFIBRILLATOR AND ACCESSORIES
  • Tipo de evento
    Recall
  • ID del evento
    17565
  • Clase de Riesgo del Evento
    II
  • Fecha de inicio del evento
    1996-04-23
  • País del evento
    Canada
  • Fuente del evento
    HC
  • Notas / Alertas
    Canadian data is current through March 2018. All of the data comes from Health Canada, 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 Canada.
  • Notas adicionales en la data
Retiro De Equipo (Recall) de ACA STAR DISCRETE CLINICAL ANALYZER
  • Tipo de evento
    Recall
  • ID del evento
    79042
  • Clase de Riesgo del Evento
    III
  • Fecha de inicio del evento
    1996-04-24
  • País del evento
    Canada
  • Fuente del evento
    HC
  • Notas / Alertas
    Canadian data is current through March 2018. All of the data comes from Health Canada, 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 Canada.
  • Notas adicionales en la data
Retiro De Equipo (Recall) de ACA STAR DISCRETE CLINICAL ANALYZER
  • Tipo de evento
    Recall
  • ID del evento
    46012
  • Clase de Riesgo del Evento
    III
  • Fecha de inicio del evento
    1996-04-24
  • País del evento
    Canada
  • Fuente del evento
    HC
  • Notas / Alertas
    Canadian data is current through March 2018. All of the data comes from Health Canada, 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 Canada.
  • Notas adicionales en la data
Retiro De Equipo (Recall) de LANDMARK VENOUS ACCESS DEVICE
  • Tipo de evento
    Recall
  • ID del evento
    33044
  • Clase de Riesgo del Evento
    II
  • Fecha de inicio del evento
    1996-04-24
  • País del evento
    Canada
  • Fuente del evento
    HC
  • Notas / Alertas
    Canadian data is current through March 2018. All of the data comes from Health Canada, 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 Canada.
  • Notas adicionales en la data
Retiro De Equipo (Recall) de BRONCHIAL DOUBLE LUMEN TUBE SET
  • Tipo de evento
    Recall
  • ID del evento
    15959
  • Clase de Riesgo del Evento
    II
  • Fecha de inicio del evento
    1996-04-25
  • País del evento
    Canada
  • Fuente del evento
    HC
  • Notas / Alertas
    Canadian data is current through March 2018. All of the data comes from Health Canada, 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 Canada.
  • Notas adicionales en la data
Retiro De Equipo (Recall) de LEGEND PLUS UNIPOLAR/BIPOLAR DUAL SENSOR SINGLE CHAMBER PACEMAKER (A...
  • Tipo de evento
    Recall
  • ID del evento
    14873
  • Clase de Riesgo del Evento
    II
  • Fecha de inicio del evento
    1996-04-29
  • País del evento
    Canada
  • Fuente del evento
    HC
  • Notas / Alertas
    Canadian data is current through March 2018. All of the data comes from Health Canada, 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 Canada.
  • Notas adicionales en la data
Retiro De Equipo (Recall) de MULTIFUNCTION ADULT ELECTRODE PADS
  • Tipo de evento
    Recall
  • ID del evento
    72876
  • Clase de Riesgo del Evento
    II
  • Fecha de inicio del evento
    1996-04-30
  • País del evento
    Canada
  • Fuente del evento
    HC
  • Notas / Alertas
    Canadian data is current through March 2018. All of the data comes from Health Canada, 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 Canada.
  • Notas adicionales en la data
Retiro De Equipo (Recall) de ACA STAR DISCRETE CLINICAL ANALYZER
  • Tipo de evento
    Recall
  • ID del evento
    41609
  • Clase de Riesgo del Evento
    III
  • Fecha de inicio del evento
    1996-04-30
  • País del evento
    Canada
  • Fuente del evento
    HC
  • Notas / Alertas
    Canadian data is current through March 2018. All of the data comes from Health Canada, 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 Canada.
  • Notas adicionales en la data
Retiro De Equipo (Recall) de KODAK EKTACHEM CLINICAL CHEMISTRY SLIDES (TRIG)
  • Tipo de evento
    Recall
  • ID del evento
    20819
  • Clase de Riesgo del Evento
    III
  • Fecha de inicio del evento
    1996-04-30
  • País del evento
    Canada
  • Fuente del evento
    HC
  • Notas / Alertas
    Canadian data is current through March 2018. All of the data comes from Health Canada, 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 Canada.
  • Notas adicionales en la data
Retiro De Equipo (Recall) de MAXIMA HOLLOW FIBRE OXYGENATOR
  • Tipo de evento
    Recall
  • ID del evento
    107263
  • Clase de Riesgo del Evento
    II
  • Fecha de inicio del evento
    1996-05-06
  • País del evento
    Canada
  • Fuente del evento
    HC
  • Notas / Alertas
    Canadian data is current through March 2018. All of the data comes from Health Canada, 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 Canada.
  • Notas adicionales en la data
Retiro De Equipo (Recall) de IL TEST TCO2
  • Tipo de evento
    Recall
  • ID del evento
    84462
  • Clase de Riesgo del Evento
    III
  • Fecha de inicio del evento
    1996-05-07
  • País del evento
    Canada
  • Fuente del evento
    HC
  • Notas / Alertas
    Canadian data is current through March 2018. All of the data comes from Health Canada, 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 Canada.
  • Notas adicionales en la data
Retiro De Equipo (Recall) de REFERRIL B CALIBRATOR
  • Tipo de evento
    Recall
  • ID del evento
    25558
  • Clase de Riesgo del Evento
    III
  • Fecha de inicio del evento
    1996-05-07
  • País del evento
    Canada
  • Fuente del evento
    HC
  • Notas / Alertas
    Canadian data is current through March 2018. All of the data comes from Health Canada, 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 Canada.
  • Notas adicionales en la data
Retiro De Equipo (Recall) de PARAMAX CUVETTES *137965
  • Tipo de evento
    Recall
  • ID del evento
    53808
  • Clase de Riesgo del Evento
    III
  • Fecha de inicio del evento
    1996-05-08
  • País del evento
    Canada
  • Fuente del evento
    HC
  • Notas / Alertas
    Canadian data is current through March 2018. All of the data comes from Health Canada, 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 Canada.
  • Notas adicionales en la data
Retiro De Equipo (Recall) de THERMALTEK WARMING STRETCHER
  • Tipo de evento
    Recall
  • ID del evento
    107502
  • Clase de Riesgo del Evento
    II
  • Fecha de inicio del evento
    1996-05-09
  • País del evento
    Canada
  • Fuente del evento
    HC
  • Notas / Alertas
    Canadian data is current through March 2018. All of the data comes from Health Canada, 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 Canada.
  • Notas adicionales en la data
Retiro De Equipo (Recall) de CANDELA CRYOTECH LCS 3000
  • Tipo de evento
    Recall
  • ID del evento
    80106
  • Clase de Riesgo del Evento
    II
  • Fecha de inicio del evento
    1996-05-09
  • País del evento
    Canada
  • Fuente del evento
    HC
  • Notas / Alertas
    Canadian data is current through March 2018. All of the data comes from Health Canada, 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 Canada.
  • Notas adicionales en la data
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