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  • Dispositivo 11
  • Fabricante 8
  • Evento 124969
  • Implante 0
Retiro De Equipo (Recall) de ACL IL TEST FIBRINOBGEN-C
  • Tipo de evento
    Recall
  • ID del evento
    48344
  • Clase de Riesgo del Evento
    III
  • 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 SYSTEM 97 (IABP) INTRA-AORTIC BALLOON PUMP
  • Tipo de evento
    Recall
  • ID del evento
    26858
  • 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 VERICORD S3
  • Tipo de evento
    Recall
  • ID del evento
    107233
  • Clase de Riesgo del Evento
    II
  • Fecha de inicio del evento
    1996-05-10
  • 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 DIMENSION DIG DIGOXIN (DIG-F)
  • Tipo de evento
    Recall
  • ID del evento
    25710
  • Clase de Riesgo del Evento
    III
  • Fecha de inicio del evento
    1996-05-10
  • 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 DIMENSION TU THYRONINE UPTAKE
  • Tipo de evento
    Recall
  • ID del evento
    105511
  • Clase de Riesgo del Evento
    III
  • Fecha de inicio del evento
    1996-05-13
  • 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 DIMENSION CLINICAL CHEMISTRY SYSTEM (INSTRUMENT)
  • Tipo de evento
    Recall
  • ID del evento
    76561
  • Clase de Riesgo del Evento
    III
  • Fecha de inicio del evento
    1996-05-13
  • 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 BELMONT ACURAY 071A DENTAL PERIAPICAL X-RAY SYSTEM
  • Tipo de evento
    Recall
  • ID del evento
    55449
  • Clase de Riesgo del Evento
    II
  • Fecha de inicio del evento
    1996-05-13
  • 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 CORPAK VTR 300 ENTERAL FEEDING PUMP
  • Tipo de evento
    Recall
  • ID del evento
    134685
  • Clase de Riesgo del Evento
    II
  • Fecha de inicio del evento
    1996-05-14
  • 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 DIMENSION CLINICAL CHEMISTRY SYSTEM (INSTRUMENT)
  • Tipo de evento
    Recall
  • ID del evento
    47922
  • Clase de Riesgo del Evento
    III
  • Fecha de inicio del evento
    1996-05-15
  • 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 WALLSTENT ESOPHAGEAL ENDOPROSTHESIS
  • Tipo de evento
    Recall
  • ID del evento
    15630
  • Clase de Riesgo del Evento
    II
  • Fecha de inicio del evento
    1996-05-15
  • 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 4C PLUS II NORMAL
  • Tipo de evento
    Recall
  • ID del evento
    75260
  • Clase de Riesgo del Evento
    III
  • Fecha de inicio del evento
    1996-05-16
  • 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 FIBRIN (OGEN) DEGRADATION PRODUCTS
  • Tipo de evento
    Recall
  • ID del evento
    76776
  • Clase de Riesgo del Evento
    III
  • Fecha de inicio del evento
    1996-05-21
  • 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 AIR SHIELDS WALL MOUNTED INFANT WARMER
  • Tipo de evento
    Recall
  • ID del evento
    108639
  • Clase de Riesgo del Evento
    III
  • Fecha de inicio del evento
    1996-05-23
  • 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 NIAGARA HIGH-FLOW IRRIGATION SYSTEM FOR BAG FLUIDS & OUTLET CONNECTORS
  • Tipo de evento
    Recall
  • ID del evento
    55909
  • Clase de Riesgo del Evento
    II
  • Fecha de inicio del evento
    1996-05-23
  • 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 SOMATOM PLUS 4C AND ACCESSORIES
  • Tipo de evento
    Recall
  • ID del evento
    109891
  • Clase de Riesgo del Evento
    II
  • Fecha de inicio del evento
    1996-05-29
  • 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 INTELLIGENT PUMP PRIMARY ADDITIVE IV SET WITH 1.2 U FILTER
  • Tipo de evento
    Recall
  • ID del evento
    65945
  • Clase de Riesgo del Evento
    II
  • Fecha de inicio del evento
    1996-05-29
  • 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 MAGNETOM EXPERT PLUS AND IMPACT PLUS
  • Tipo de evento
    Recall
  • ID del evento
    27285
  • Clase de Riesgo del Evento
    II
  • Fecha de inicio del evento
    1996-05-29
  • 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 HANAULUX 2007 OPT. SATELLITE (OPERATING ROOM LIGHT)
  • Tipo de evento
    Recall
  • ID del evento
    20164
  • Clase de Riesgo del Evento
    II
  • Fecha de inicio del evento
    1996-05-29
  • 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 ACL IL TEST LAC SCREEN
  • Tipo de evento
    Recall
  • ID del evento
    81726
  • Clase de Riesgo del Evento
    III
  • Fecha de inicio del evento
    1996-05-30
  • 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 IL TEST LAC CONFIRM
  • Tipo de evento
    Recall
  • ID del evento
    16042
  • Clase de Riesgo del Evento
    III
  • Fecha de inicio del evento
    1996-05-30
  • 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 CMVSCAN CARD TEST KIT
  • Tipo de evento
    Recall
  • ID del evento
    17205
  • Clase de Riesgo del Evento
    III
  • Fecha de inicio del evento
    1996-05-31
  • 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 VALTRAC BIOFRAGMENTABLE ANASTOMOSIS RINGS
  • Tipo de evento
    Recall
  • ID del evento
    86446
  • Clase de Riesgo del Evento
    II
  • Fecha de inicio del evento
    1996-06-03
  • 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 FRESENIUS 2008H HEMODIALYSIS MACHINE
  • Tipo de evento
    Recall
  • ID del evento
    109653
  • Clase de Riesgo del Evento
    II
  • Fecha de inicio del evento
    1996-06-11
  • 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 LYSE S II
  • Tipo de evento
    Recall
  • ID del evento
    96791
  • Clase de Riesgo del Evento
    III
  • Fecha de inicio del evento
    1996-06-11
  • 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-TRACE ECG CONDUCTIVE ADHESIVE MONITORING ELECTRODES
  • Tipo de evento
    Recall
  • ID del evento
    52862
  • Clase de Riesgo del Evento
    II
  • Fecha de inicio del evento
    1996-06-12
  • 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
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