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  • Dispositivo 2
  • Fabricante 2
  • Evento 124969
  • Implante 0
Retiro De Equipo (Recall) de “Non-sterile gauze medical bandage 5m x 10cm”, date of manufacture 2...
  • Tipo de evento
    Recall
  • ID del evento
    01И-2136/16,
  • Fecha
    2016-11-01
  • Fecha de publicación del evento
    2016-11-01
  • País del evento
    Russian Federation
  • Fuente del evento
    FSSH
  • URL de la fuente del evento
    http://www.roszdravnadzor.ru/services/unreg
  • Notas / Alertas
    Russian data is current through January 2019. All of the data comes from the Federal Service for Surveillance in Healthcare, 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 Russia.
  • Notas adicionales en la data
    Manufacturer Recall
Retiro De Equipo (Recall) de Small dental instrument sterilizer electric with glass balls SS-01 "...
  • Tipo de evento
    Recall
  • ID del evento
    02И-2041/17,
  • Número del evento
    01И-1583/17
  • Fecha
    2017-08-18
  • Fecha de publicación del evento
    2017-08-21
  • País del evento
    Russian Federation
  • Fuente del evento
    FSSH
  • URL de la fuente del evento
    http://www.roszdravnadzor.ru/services/unreg
  • Notas / Alertas
    Russian data is current through January 2019. All of the data comes from the Federal Service for Surveillance in Healthcare, 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 Russia.
  • Notas adicionales en la data
    Manufacturer Recall
Retiro De Equipo (Recall) de Instruments for cardiovascular surgery
  • Tipo de evento
    Recall
  • ID del evento
    01И-1651/14,
  • Fecha
    2014-10-22
  • Fecha de publicación del evento
    2014-10-27
  • País del evento
    Russian Federation
  • Fuente del evento
    FSSH
  • URL de la fuente del evento
    http://www.roszdravnadzor.ru/services/unreg
  • Notas / Alertas
    Russian data is current through January 2019. All of the data comes from the Federal Service for Surveillance in Healthcare, 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 Russia.
  • Notas adicionales en la data
    Manufacturer Recall
Retiro De Equipo (Recall) de Reagents for in vitro determination of biochemical blood parameters ...
  • Tipo de evento
    Recall
  • ID del evento
    01И-2167/15, ФСЗ 2008/01122
  • Fecha
    2015-12-16
  • Fecha de publicación del evento
    2015-12-16
  • País del evento
    Russian Federation
  • Fuente del evento
    FSSH
  • URL de la fuente del evento
    http://www.roszdravnadzor.ru/services/unreg
  • Notas / Alertas
    Russian data is current through January 2019. All of the data comes from the Federal Service for Surveillance in Healthcare, 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 Russia.
  • Notas adicionales en la data
    Manufacturer Recall
Retiro De Equipo (Recall) de Sterile single-use polymer bags for taking, storing and transporting...
  • Tipo de evento
    Recall
  • ID del evento
    01И-2730/18, ФСЗ 2011/11150
  • Número del evento
    01И-2223/18
  • Fecha
    2018-11-19
  • Fecha de publicación del evento
    2018-11-19
  • País del evento
    Russian Federation
  • Fuente del evento
    FSSH
  • URL de la fuente del evento
    http://www.roszdravnadzor.ru/services/unreg
  • Notas / Alertas
    Russian data is current through January 2019. All of the data comes from the Federal Service for Surveillance in Healthcare, 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 Russia.
  • Notas adicionales en la data
    Manufacturer Recall
Retiro De Equipo (Recall) de Injection syringe with needle, HELMJECT®
  • Tipo de evento
    Recall
  • ID del evento
    01И-1333/18, ФСЗ 2008/00033
  • Número del evento
    01И-269/18
  • Fecha
    2018-05-29
  • Fecha de publicación del evento
    2018-05-30
  • País del evento
    Russian Federation
  • Fuente del evento
    FSSH
  • URL de la fuente del evento
    http://www.roszdravnadzor.ru/services/unreg
  • Notas / Alertas
    Russian data is current through January 2019. All of the data comes from the Federal Service for Surveillance in Healthcare, 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 Russia.
  • Notas adicionales en la data
    Manufacturer Recall
Retiro De Equipo (Recall) de Catgut plain polished sterile, with needles and without needles
  • Tipo de evento
    Recall
  • ID del evento
    01И-1047/18, ФСЗ 2008/00032
  • Fecha
    2018-04-27
  • Fecha de publicación del evento
    2018-05-03
  • País del evento
    Russian Federation
  • Fuente del evento
    FSSH
  • URL de la fuente del evento
    http://www.roszdravnadzor.ru/services/unreg
  • Notas / Alertas
    Russian data is current through January 2019. All of the data comes from the Federal Service for Surveillance in Healthcare, 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 Russia.
  • Notas adicionales en la data
    Manufacturer Recall
Retiro De Equipo (Recall) de Foley catheter balloon latex siliconized
  • Tipo de evento
    Recall
  • ID del evento
    01И-2187/17, ФСЗ 2009/04020
  • Número del evento
    01И-1178/15
  • Fecha
    2017-09-05
  • Fecha de publicación del evento
    2017-09-06
  • País del evento
    Russian Federation
  • Fuente del evento
    FSSH
  • URL de la fuente del evento
    http://www.roszdravnadzor.ru/services/unreg
  • Notas / Alertas
    Russian data is current through January 2019. All of the data comes from the Federal Service for Surveillance in Healthcare, 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 Russia.
  • Notas adicionales en la data
    Manufacturer Recall
Retiro De Equipo (Recall) de Disposable intravenous catheter
  • Tipo de evento
    Recall
  • ID del evento
    01И-2816/18, ФСЗ 2008/02981
  • Número del evento
    01И-1898/18
  • Fecha
    2018-11-27
  • Fecha de publicación del evento
    2018-11-28
  • País del evento
    Russian Federation
  • Fuente del evento
    FSSH
  • URL de la fuente del evento
    http://www.roszdravnadzor.ru/services/unreg
  • Notas / Alertas
    Russian data is current through January 2019. All of the data comes from the Federal Service for Surveillance in Healthcare, 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 Russia.
  • Notas adicionales en la data
    Manufacturer Recall
Retiro De Equipo (Recall) de Medical polymer products for anaesthesiology and resuscitation (see ...
  • Tipo de evento
    Recall
  • ID del evento
    01И-1210/18, ФСЗ 2011/10317
  • Número del evento
    01И-504/18
  • Fecha
    2018-05-11
  • Fecha de publicación del evento
    2018-05-14
  • País del evento
    Russian Federation
  • Fuente del evento
    FSSH
  • URL de la fuente del evento
    http://www.roszdravnadzor.ru/services/unreg
  • Notas / Alertas
    Russian data is current through January 2019. All of the data comes from the Federal Service for Surveillance in Healthcare, 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 Russia.
  • Notas adicionales en la data
    Manufacturer Recall
Retiro De Equipo (Recall) de Medical polymer products for anaesthesiology and resuscitation (see ...
  • Tipo de evento
    Recall
  • ID del evento
    01И-1018/18, ФСЗ 2011/10317
  • Número del evento
    01И-578/18
  • Fecha
    2018-04-26
  • Fecha de publicación del evento
    2018-04-27
  • País del evento
    Russian Federation
  • Fuente del evento
    FSSH
  • URL de la fuente del evento
    http://www.roszdravnadzor.ru/services/unreg
  • Notas / Alertas
    Russian data is current through January 2019. All of the data comes from the Federal Service for Surveillance in Healthcare, 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 Russia.
  • Notas adicionales en la data
    Manufacturer Recall
Retiro De Equipo (Recall) de Coronary stent MGuard Prime with delivery system
  • Tipo de evento
    Recall
  • ID del evento
    01И-1316/14,
  • Fecha
    2014-08-28
  • Fecha de publicación del evento
    2014-08-29
  • País del evento
    Russian Federation
  • Fuente del evento
    FSSH
  • URL de la fuente del evento
    http://www.roszdravnadzor.ru/services/unreg
  • Notas / Alertas
    Russian data is current through January 2019. All of the data comes from the Federal Service for Surveillance in Healthcare, 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 Russia.
  • Notas adicionales en la data
    Manufacturer Recall
Retiro De Equipo (Recall) de DuraGen, DuraGen Plus, Suturable DuraGen Plastic Implants
  • Tipo de evento
    Recall
  • ID del evento
    01И-2389/18, ФСЗ 2011/09820
  • Fecha
    2018-10-09
  • Fecha de publicación del evento
    2018-10-10
  • País del evento
    Russian Federation
  • Fuente del evento
    FSSH
  • URL de la fuente del evento
    http://www.roszdravnadzor.ru/services/unreg
  • Notas / Alertas
    Russian data is current through January 2019. All of the data comes from the Federal Service for Surveillance in Healthcare, 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 Russia.
  • Notas adicionales en la data
    Manufacturer Recall
Retiro De Equipo (Recall) de Barrier Easy Warm Patient Heating Blanket with Active Self Heating T...
  • Tipo de evento
    Recall
  • ID del evento
    01И-1/16, РЗН 2013/780
  • Fecha
    2016-01-11
  • Fecha de publicación del evento
    2016-01-12
  • País del evento
    Russian Federation
  • Fuente del evento
    FSSH
  • URL de la fuente del evento
    http://www.roszdravnadzor.ru/services/unreg
  • Notas / Alertas
    Russian data is current through January 2019. All of the data comes from the Federal Service for Surveillance in Healthcare, 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 Russia.
  • Notas adicionales en la data
    Manufacturer Recall
Retiro De Equipo (Recall) de Probe urogenital disposable Dafina-Alayf (see Annex on 1 sheet)
  • Tipo de evento
    Recall
  • ID del evento
    01И-2471/18, ФСЗ 2010/07224
  • Número del evento
    01И-1502/18
  • Fecha
    2018-10-22
  • Fecha de publicación del evento
    2018-10-22
  • País del evento
    Russian Federation
  • Fuente del evento
    FSSH
  • URL de la fuente del evento
    http://www.roszdravnadzor.ru/services/unreg
  • Notas / Alertas
    Russian data is current through January 2019. All of the data comes from the Federal Service for Surveillance in Healthcare, 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 Russia.
  • Notas adicionales en la data
    Manufacturer Recall
Retiro De Equipo (Recall) de Calaprike APEXMED
  • Tipo de evento
    Recall
  • ID del evento
    01И-1877/18, ФСЗ 2009/05780
  • Número del evento
    01И-1739/18
  • Fecha
    2018-08-03
  • Fecha de publicación del evento
    2018-08-06
  • País del evento
    Russian Federation
  • Fuente del evento
    FSSH
  • URL de la fuente del evento
    http://www.roszdravnadzor.ru/services/unreg
  • Notas / Alertas
    Russian data is current through January 2019. All of the data comes from the Federal Service for Surveillance in Healthcare, 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 Russia.
  • Notas adicionales en la data
    Manufacturer Recall
Retiro De Equipo (Recall) de Test tubes for vacuum sampling, storage and transportation of blood ...
  • Tipo de evento
    Recall
  • ID del evento
    01И-1325/18, ФСЗ 2011/09178
  • Fecha
    2018-05-29
  • Fecha de publicación del evento
    2018-06-05
  • País del evento
    Russian Federation
  • Fuente del evento
    FSSH
  • URL de la fuente del evento
    http://www.roszdravnadzor.ru/services/unreg
  • Notas / Alertas
    Russian data is current through January 2019. All of the data comes from the Federal Service for Surveillance in Healthcare, 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 Russia.
  • Notas adicionales en la data
    Manufacturer Recall
Retiro De Equipo (Recall) de Test tubes for vacuum sampling, storage and transportation of blood ...
  • Tipo de evento
    Recall
  • ID del evento
    01И-2813/17, ФСЗ 2011/09178
  • Número del evento
    02И-2008/17
  • Fecha
    2017-11-13
  • Fecha de publicación del evento
    2017-11-14
  • País del evento
    Russian Federation
  • Fuente del evento
    FSSH
  • URL de la fuente del evento
    http://www.roszdravnadzor.ru/services/unreg
  • Notas / Alertas
    Russian data is current through January 2019. All of the data comes from the Federal Service for Surveillance in Healthcare, 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 Russia.
  • Notas adicionales en la data
    Manufacturer Recall
Retiro De Equipo (Recall) de The adhesive plaster LEIKO fixing medical
  • Tipo de evento
    Recall
  • ID del evento
    01И-353/16, ФСЗ 2008/01442
  • Fecha
    2016-02-20
  • Fecha de publicación del evento
    2016-02-26
  • País del evento
    Russian Federation
  • Fuente del evento
    FSSH
  • URL de la fuente del evento
    http://www.roszdravnadzor.ru/services/unreg
  • Notas / Alertas
    Russian data is current through January 2019. All of the data comes from the Federal Service for Surveillance in Healthcare, 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 Russia.
  • Notas adicionales en la data
    Manufacturer Recall
Retiro De Equipo (Recall) de Adhesive plaster LEIKO (LEIKO) bactericidal
  • Tipo de evento
    Recall
  • ID del evento
    01И-1334/18, ФСЗ 2008/01495
  • Número del evento
    01И-1068/18
  • Fecha
    2018-05-29
  • Fecha de publicación del evento
    2018-05-30
  • País del evento
    Russian Federation
  • Fuente del evento
    FSSH
  • URL de la fuente del evento
    http://www.roszdravnadzor.ru/services/unreg
  • Notas / Alertas
    Russian data is current through January 2019. All of the data comes from the Federal Service for Surveillance in Healthcare, 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 Russia.
  • Notas adicionales en la data
    Manufacturer Recall
Retiro De Equipo (Recall) de The adhesive LEIKO plaster (LEIKO) fixing medical
  • Tipo de evento
    Recall
  • ID del evento
    01И-1200/18, ФСЗ 2008/01442
  • Número del evento
    01И-742/18
  • Fecha
    2018-05-11
  • Fecha de publicación del evento
    2018-05-22
  • País del evento
    Russian Federation
  • Fuente del evento
    FSSH
  • URL de la fuente del evento
    http://www.roszdravnadzor.ru/services/unreg
  • Notas / Alertas
    Russian data is current through January 2019. All of the data comes from the Federal Service for Surveillance in Healthcare, 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 Russia.
  • Notas adicionales en la data
    Manufacturer Recall
Retiro De Equipo (Recall) de The adhesive LEIKO plaster (LEIKO) fixing medical
  • Tipo de evento
    Recall
  • ID del evento
    01И-829/18, ФСЗ 2008/01442
  • Número del evento
    01И-473/18
  • Fecha
    2018-04-03
  • Fecha de publicación del evento
    2018-04-03
  • País del evento
    Russian Federation
  • Fuente del evento
    FSSH
  • URL de la fuente del evento
    http://www.roszdravnadzor.ru/services/unreg
  • Notas / Alertas
    Russian data is current through January 2019. All of the data comes from the Federal Service for Surveillance in Healthcare, 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 Russia.
  • Notas adicionales en la data
    Manufacturer Recall
Retiro De Equipo (Recall) de Urogenital disposable sterile probes (see Annex on 1 sheet)
  • Tipo de evento
    Recall
  • ID del evento
    01И-1336/18, ФСЗ 2011/10587
  • Número del evento
    01И-871/18
  • Fecha
    2018-05-29
  • Fecha de publicación del evento
    2018-05-30
  • País del evento
    Russian Federation
  • Fuente del evento
    FSSH
  • URL de la fuente del evento
    http://www.roszdravnadzor.ru/services/unreg
  • Notas / Alertas
    Russian data is current through January 2019. All of the data comes from the Federal Service for Surveillance in Healthcare, 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 Russia.
  • Notas adicionales en la data
    Manufacturer Recall
Retiro De Equipo (Recall) de Urogenital disposable sterile probes (see Annex on 1 sheet)
  • Tipo de evento
    Recall
  • ID del evento
    01И-1337/18, ФСЗ 2011/10587
  • Número del evento
    01И-817/18
  • Fecha
    2018-05-29
  • Fecha de publicación del evento
    2018-05-30
  • País del evento
    Russian Federation
  • Fuente del evento
    FSSH
  • URL de la fuente del evento
    http://www.roszdravnadzor.ru/services/unreg
  • Notas / Alertas
    Russian data is current through January 2019. All of the data comes from the Federal Service for Surveillance in Healthcare, 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 Russia.
  • Notas adicionales en la data
    Manufacturer Recall
Retiro De Equipo (Recall) de Urogenital disposable sterile probes (see Annex on 1 sheet)
  • Tipo de evento
    Recall
  • ID del evento
    01И-1338/18, ФСЗ 2011/10587
  • Número del evento
    01И-3318/17
  • Fecha
    2018-05-29
  • Fecha de publicación del evento
    2018-05-30
  • País del evento
    Russian Federation
  • Fuente del evento
    FSSH
  • URL de la fuente del evento
    http://www.roszdravnadzor.ru/services/unreg
  • Notas / Alertas
    Russian data is current through January 2019. All of the data comes from the Federal Service for Surveillance in Healthcare, 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 Russia.
  • Notas adicionales en la data
    Manufacturer Recall
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Acerca de la base de datos

Explore más de 120,000 registros de retiros, alertas y notificaciones de seguridad de dispositivos médicos y sus conexiones con los fabricantes.

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Aviso

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.

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