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  • Dispositivo 75
  • Fabricante 75
  • Evento 75
  • Implante 0
Retiro De Equipo (Recall) de PEDIATRIC NEBULIZER MASK
  • Tipo de evento
    Recall
  • Fecha
    2015-07-13
  • País del evento
    Tunisia
  • Fuente del evento
    DPMT
  • URL de la fuente del evento
    http://www.dpm.tn/
  • Notas / Alertas
    Tunisian data is current through December 2018. All of the data comes from DPM Tunisie, 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 Tunisia.
  • Notas adicionales en la data
    Country: Turkey
Retiro De Equipo (Recall) de ADULT NEBULIZER MASK
  • Tipo de evento
    Recall
  • Fecha
    2015-07-13
  • País del evento
    Tunisia
  • Fuente del evento
    DPMT
  • URL de la fuente del evento
    http://www.dpm.tn/
  • Notas / Alertas
    Tunisian data is current through December 2018. All of the data comes from DPM Tunisie, 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 Tunisia.
  • Notas adicionales en la data
    Country: Turkey
Retiro De Equipo (Recall) de POWDERED SURGICAL GLOVES N°8
  • Tipo de evento
    Recall
  • Fecha
    2015-06-13
  • País del evento
    Tunisia
  • Fuente del evento
    DPMT
  • URL de la fuente del evento
    http://www.dpm.tn/
  • Notas / Alertas
    Tunisian data is current through December 2018. All of the data comes from DPM Tunisie, 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 Tunisia.
  • Notas adicionales en la data
    Country: Malaysia
Retiro De Equipo (Recall) de Syringe 3 ml
  • Tipo de evento
    Recall
  • Fecha
    2013-01-10
  • País del evento
    Tunisia
  • Fuente del evento
    DPMT
  • URL de la fuente del evento
    http://www.dpm.tn/
  • Notas / Alertas
    Tunisian data is current through December 2018. All of the data comes from DPM Tunisie, 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 Tunisia.
  • Notas adicionales en la data
    Country: Tunisia
Retiro De Equipo (Recall) de INTRA VENOUS CATHETER 20G
  • Tipo de evento
    Recall
  • Fecha
    2014-09-29
  • País del evento
    Tunisia
  • Fuente del evento
    DPMT
  • URL de la fuente del evento
    http://www.dpm.tn/
  • Notas / Alertas
    Tunisian data is current through December 2018. All of the data comes from DPM Tunisie, 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 Tunisia.
  • Notas adicionales en la data
    Country: Tunisia
Retiro De Equipo (Recall) de BLOOD TRANSFER DEVICE
  • Tipo de evento
    Recall
  • Fecha
    2015-02-27
  • País del evento
    Tunisia
  • Fuente del evento
    DPMT
  • URL de la fuente del evento
    http://www.dpm.tn/
  • Notas / Alertas
    Tunisian data is current through December 2018. All of the data comes from DPM Tunisie, 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 Tunisia.
  • Notas adicionales en la data
    Country: Tunisia
Retiro De Equipo (Recall) de MAYO TUBE N°1
  • Tipo de evento
    Recall
  • Fecha
    2012-05-29
  • País del evento
    Tunisia
  • Fuente del evento
    DPMT
  • URL de la fuente del evento
    http://www.dpm.tn/
  • Notas / Alertas
    Tunisian data is current through December 2018. All of the data comes from DPM Tunisie, 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 Tunisia.
  • Notas adicionales en la data
    Country: Tunisia
Retiro De Equipo (Recall) de BUTTERFLY NEEDLE 22G
  • Tipo de evento
    Recall
  • Fecha
    2012-05-29
  • País del evento
    Tunisia
  • Fuente del evento
    DPMT
  • URL de la fuente del evento
    http://www.dpm.tn/
  • Notas / Alertas
    Tunisian data is current through December 2018. All of the data comes from DPM Tunisie, 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 Tunisia.
  • Notas adicionales en la data
    Country: Tunisia
Retiro De Equipo (Recall) de SUCTION CATHETER CH 16
  • Tipo de evento
    Recall
  • Fecha
    2012-05-29
  • País del evento
    Tunisia
  • Fuente del evento
    DPMT
  • URL de la fuente del evento
    http://www.dpm.tn/
  • Notas / Alertas
    Tunisian data is current through December 2018. All of the data comes from DPM Tunisie, 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 Tunisia.
  • Notas adicionales en la data
    Country: Tunisia
Retiro De Equipo (Recall) de TRACHEAL INTUBATION CATHETER 4.5MM
  • Tipo de evento
    Recall
  • Fecha
    2012-05-29
  • País del evento
    Tunisia
  • Fuente del evento
    DPMT
  • URL de la fuente del evento
    http://www.dpm.tn/
  • Notas / Alertas
    Tunisian data is current through December 2018. All of the data comes from DPM Tunisie, 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 Tunisia.
  • Notas adicionales en la data
    Country: Tunisia
Retiro De Equipo (Recall) de TRACHEAL INTUBATION CATHETER WITHOUT BALLOON 5.5MM
  • Tipo de evento
    Recall
  • Fecha
    2012-05-29
  • País del evento
    Tunisia
  • Fuente del evento
    DPMT
  • URL de la fuente del evento
    http://www.dpm.tn/
  • Notas / Alertas
    Tunisian data is current through December 2018. All of the data comes from DPM Tunisie, 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 Tunisia.
  • Notas adicionales en la data
    Country: Tunisia
Retiro De Equipo (Recall) de FOLEY CATHETER CH 16
  • Tipo de evento
    Recall
  • Fecha
    2012-05-29
  • País del evento
    Tunisia
  • Fuente del evento
    DPMT
  • URL de la fuente del evento
    http://www.dpm.tn/
  • Notas / Alertas
    Tunisian data is current through December 2018. All of the data comes from DPM Tunisie, 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 Tunisia.
  • Notas adicionales en la data
    Country: Tunisia
Retiro De Equipo (Recall) de PENIS CASE DIAMETER 25
  • Tipo de evento
    Recall
  • Fecha
    2012-05-29
  • País del evento
    Tunisia
  • Fuente del evento
    DPMT
  • URL de la fuente del evento
    http://www.dpm.tn/
  • Notas / Alertas
    Tunisian data is current through December 2018. All of the data comes from DPM Tunisie, 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 Tunisia.
  • Notas adicionales en la data
    Country: Tunisia
Retiro De Equipo (Recall) de VANGUARD FEMORAL IMPLANT
  • Tipo de evento
    Recall
  • Fecha
    2017-02-22
  • País del evento
    Tunisia
  • Fuente del evento
    DPMT
  • URL de la fuente del evento
    http://www.dpm.tn/
  • Notas / Alertas
    Tunisian data is current through December 2018. All of the data comes from DPM Tunisie, 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 Tunisia.
  • Notas adicionales en la data
    Country: Tunisia
  • Causa
    "the packaging of some femoral implants is incorrectly labeled".
Retiro De Equipo (Recall) de FORFENAN
  • Tipo de evento
    Recall
  • Fecha
    2016-03-22
  • País del evento
    Tunisia
  • Fuente del evento
    DPMT
  • URL de la fuente del evento
    http://www.dpm.tn/
  • Notas / Alertas
    Tunisian data is current through December 2018. All of the data comes from DPM Tunisie, 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 Tunisia.
  • Notas adicionales en la data
Retiro De Equipo (Recall) de UMBILICAL CLAMPS
  • Tipo de evento
    Recall
  • Fecha
    2015-11-04
  • País del evento
    Tunisia
  • Fuente del evento
    DPMT
  • URL de la fuente del evento
    http://www.dpm.tn/
  • Notas / Alertas
    Tunisian data is current through December 2018. All of the data comes from DPM Tunisie, 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 Tunisia.
  • Notas adicionales en la data
    Country: India
Retiro De Equipo (Recall) de ACID CONCENTRATE for hemodialysis Ca2 + FL / 10L
  • Tipo de evento
    Recall
  • Fecha
    2013-09-06
  • País del evento
    Tunisia
  • Fuente del evento
    DPMT
  • URL de la fuente del evento
    http://www.dpm.tn/
  • Notas / Alertas
    Tunisian data is current through December 2018. All of the data comes from DPM Tunisie, 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 Tunisia.
  • Notas adicionales en la data
    Country: Tunisia
Retiro De Equipo (Recall) de ACID CONCENTRATE for hemodialysis FL / 200ml
  • Tipo de evento
    Recall
  • Fecha
    2013-09-06
  • País del evento
    Tunisia
  • Fuente del evento
    DPMT
  • URL de la fuente del evento
    http://www.dpm.tn/
  • Notas / Alertas
    Tunisian data is current through December 2018. All of the data comes from DPM Tunisie, 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 Tunisia.
  • Notas adicionales en la data
    Country: Tunisia
Retiro De Equipo (Recall) de ACID CONCENTRATE for hemodialysis FL / 10L
  • Tipo de evento
    Recall
  • Fecha
    2013-09-06
  • País del evento
    Tunisia
  • Fuente del evento
    DPMT
  • URL de la fuente del evento
    http://www.dpm.tn/
  • Notas / Alertas
    Tunisian data is current through December 2018. All of the data comes from DPM Tunisie, 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 Tunisia.
  • Notas adicionales en la data
    Country: Tunisia
Retiro De Equipo (Recall) de CATHETERS GUIDE 6F
  • Tipo de evento
    Recall
  • Fecha
    2016-02-10
  • País del evento
    Tunisia
  • Fuente del evento
    DPMT
  • URL de la fuente del evento
    http://www.dpm.tn/
  • Notas / Alertas
    Tunisian data is current through December 2018. All of the data comes from DPM Tunisie, 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 Tunisia.
  • Notas adicionales en la data
    Country: Netherlands
Retiro De Equipo (Recall) de CH8 SUCTION CATHETER, CH10 SUCTION CATHETER AND CH12 SUCTION CATHETER
  • Tipo de evento
    Recall
  • Fecha
    2015-12-02
  • País del evento
    Tunisia
  • Fuente del evento
    DPMT
  • URL de la fuente del evento
    http://www.dpm.tn/
  • Notas / Alertas
    Tunisian data is current through December 2018. All of the data comes from DPM Tunisie, 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 Tunisia.
  • Notas adicionales en la data
    Country: CHINA
Retiro De Equipo (Recall) de CH4 SUCTION CATHETER
  • Tipo de evento
    Recall
  • Fecha
    2016-01-13
  • País del evento
    Tunisia
  • Fuente del evento
    DPMT
  • URL de la fuente del evento
    http://www.dpm.tn/
  • Notas / Alertas
    Tunisian data is current through December 2018. All of the data comes from DPM Tunisie, 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 Tunisia.
  • Notas adicionales en la data
    Country: CHINA
Retiro De Equipo (Recall) de ADULT NEBULIZER MASK
  • Tipo de evento
    Recall
  • Fecha
    2015-10-08
  • País del evento
    Tunisia
  • Fuente del evento
    DPMT
  • URL de la fuente del evento
    http://www.dpm.tn/
  • Notas / Alertas
    Tunisian data is current through December 2018. All of the data comes from DPM Tunisie, 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 Tunisia.
  • Notas adicionales en la data
    Country: Turkey
Retiro De Equipo (Recall) de NON-STERILE LAPARATOMY SPONGE 50x40cm 17 threads / cm2
  • Tipo de evento
    Recall
  • Fecha
    2015-01-15
  • País del evento
    Tunisia
  • Fuente del evento
    DPMT
  • URL de la fuente del evento
    http://www.dpm.tn/
  • Notas / Alertas
    Tunisian data is current through December 2018. All of the data comes from DPM Tunisie, 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 Tunisia.
  • Notas adicionales en la data
    Country: Tunisia
Retiro De Equipo (Recall) de Stretch Woven Gauze Bandage 7cmX4m
  • Tipo de evento
    Recall
  • Fecha
    2015-01-15
  • País del evento
    Tunisia
  • Fuente del evento
    DPMT
  • URL de la fuente del evento
    http://www.dpm.tn/
  • Notas / Alertas
    Tunisian data is current through December 2018. All of the data comes from DPM Tunisie, 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 Tunisia.
  • Notas adicionales en la data
    Country: Tunisia
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Los dispositivos médicos ayudan con el diagnóstico, la prevención y el tratamiento de muchas lesiones y enfermedades. A través de la International Medical Devices Database no estamos sugiriendo que compañías u otras entidades mencionadas en la base de datos hayan sido parte de una conducta ilegal o hayan actuado de manera impropia. Un mismo dispositivo médico puede tener distintos nombres en diferentes países. Esta base de datos no busca proporcionar asesoría médica. Los pacientes deben consultar con sus médicos para determinar si la data contiene información relevante y si la misma tiene implicaciones médicas para ellos.