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  • Dispositivo 152
  • Fabricante 61
  • Evento 124969
  • Implante 0
Retiro De Equipo (Recall) de NEWPORT BREEZE VENTILATOR
  • Tipo de evento
    Recall
  • ID del evento
    132098
  • Clase de Riesgo del Evento
    II
  • Fecha de inicio del evento
    1991-08-07
  • 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 INTELLIGENT PUMP
  • Tipo de evento
    Recall
  • ID del evento
    33345
  • Clase de Riesgo del Evento
    II
  • Fecha de inicio del evento
    1992-04-03
  • 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 ARTHRO-FLOW IRRIGATOR
  • Tipo de evento
    Recall
  • ID del evento
    30748
  • Clase de Riesgo del Evento
    II
  • Fecha de inicio del evento
    1992-10-28
  • 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 LP10 VOLUME VENTILATOR
  • Tipo de evento
    Recall
  • ID del evento
    23847
  • Clase de Riesgo del Evento
    II
  • Fecha de inicio del evento
    1993-12-21
  • 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 FLO-GARD 6201 VOLUMETRIC INFUSION PUMP
  • Tipo de evento
    Recall
  • ID del evento
    127834
  • Clase de Riesgo del Evento
    II
  • Fecha de inicio del evento
    1994-01-11
  • 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 FLO-GARD 6301 DUAL-CHANNEL VOLUMETRIC INFUSION PUMP
  • Tipo de evento
    Recall
  • ID del evento
    104711
  • Clase de Riesgo del Evento
    II
  • Fecha de inicio del evento
    1994-01-11
  • 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 AUTO SYRINGE INFUSION PUMP - MODEL AS50A
  • Tipo de evento
    Recall
  • ID del evento
    25806
  • Clase de Riesgo del Evento
    III
  • Fecha de inicio del evento
    1994-04-18
  • 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 BLOOD WARMER *
  • Tipo de evento
    Recall
  • ID del evento
    25580
  • Clase de Riesgo del Evento
    II
  • Fecha de inicio del evento
    1994-07-20
  • 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 VICRYL (POLYGLACTIN 910) ABSORBABLE SUTURES
  • Tipo de evento
    Recall
  • ID del evento
    31874
  • Clase de Riesgo del Evento
    II
  • Fecha de inicio del evento
    1994-09-14
  • 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 KODAK MIN-R XRAY FILM
  • Tipo de evento
    Recall
  • ID del evento
    69394
  • Clase de Riesgo del Evento
    II
  • Fecha de inicio del evento
    1994-09-19
  • 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 VITRECTOMY PACK *154660 154661
  • Tipo de evento
    Recall
  • ID del evento
    79537
  • Clase de Riesgo del Evento
    II
  • Fecha de inicio del evento
    1994-11-02
  • 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 QUICK ABG SAMPLER
  • Tipo de evento
    Recall
  • ID del evento
    85385
  • Clase de Riesgo del Evento
    II
  • Fecha de inicio del evento
    1994-12-29
  • 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
  • Causa
    Mfr has determined that after use the needles have a potential for inadvertent withdrawal (backing out) from the stopper cube used for disposal. it is important that universal precautions be utilized for spec.
Retiro De Equipo (Recall) de RESPONDER 1200 DEFIBRILLATOR
  • Tipo de evento
    Recall
  • ID del evento
    130696
  • Clase de Riesgo del Evento
    I
  • Fecha de inicio del evento
    1995-01-23
  • 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 RESPONDER 1500
  • Tipo de evento
    Recall
  • ID del evento
    43251
  • Clase de Riesgo del Evento
    I
  • Fecha de inicio del evento
    1995-01-23
  • 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 KODAK MIN-R XRAY FILM
  • Tipo de evento
    Recall
  • ID del evento
    43310
  • Clase de Riesgo del Evento
    II
  • Fecha de inicio del evento
    1995-01-26
  • 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 CT 9000 CONTRAST DELIVERY SYSTEM - INJECTOR
  • Tipo de evento
    Recall
  • ID del evento
    21149
  • Clase de Riesgo del Evento
    I
  • Fecha de inicio del evento
    1995-02-21
  • 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 STRATUS FMMZ DIGOXIN KIT
  • Tipo de evento
    Recall
  • ID del evento
    32309
  • Clase de Riesgo del Evento
    III
  • Fecha de inicio del evento
    1995-03-21
  • 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 STRATUS FMMZ DIGOXIN KIT
  • Tipo de evento
    Recall
  • ID del evento
    51873
  • Clase de Riesgo del Evento
    III
  • Fecha de inicio del evento
    1995-03-24
  • 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 BLOOD BANK QUALITY ASSURANCE TESTING REAGENTS
  • Tipo de evento
    Recall
  • ID del evento
    31034
  • Clase de Riesgo del Evento
    III
  • Fecha de inicio del evento
    1995-03-24
  • 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 REVERSE-CYTE REAGENT RED BLOOD CELL
  • Tipo de evento
    Recall
  • ID del evento
    19674
  • Clase de Riesgo del Evento
    III
  • Fecha de inicio del evento
    1995-03-24
  • 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 NEER 2 TOTAL SHOULDER METAL BACKED GLENOID
  • Tipo de evento
    Recall
  • ID del evento
    49937
  • Clase de Riesgo del Evento
    II
  • Fecha de inicio del evento
    1995-04-06
  • 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 PARAMAX CSF/URINE PROTEIN REAGENT
  • Tipo de evento
    Recall
  • ID del evento
    53236
  • Clase de Riesgo del Evento
    III
  • Fecha de inicio del evento
    1995-05-01
  • 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 MERCURIAL SPHYGMOMANOMETERS (BLOOD PRESSURE CUFFS)
  • Tipo de evento
    Recall
  • ID del evento
    27266
  • Clase de Riesgo del Evento
    III
  • Fecha de inicio del evento
    1995-06-08
  • 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 FILSHIE CLIP SYSTEM
  • Tipo de evento
    Recall
  • ID del evento
    84987
  • Clase de Riesgo del Evento
    II
  • Fecha de inicio del evento
    1995-06-13
  • 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 MEDI-MAN PATIENT LIFTER
  • Tipo de evento
    Recall
  • ID del evento
    12359
  • Clase de Riesgo del Evento
    III
  • Fecha de inicio del evento
    1995-09-19
  • 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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