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  • Dispositivo 124
  • Fabricante 32
  • Evento 124969
  • Implante 6
Notificaciones De Seguridad De Campo acerca de Check-Flo® Hemostasis Unit, Flexor® Radial Access ...
  • Tipo de evento
    Field Safety Notice
  • ID del evento
    2017/193 & 2017FA0002
  • Fecha
    2017-02-15
  • País del evento
    Turkey
  • Fuente del evento
    TDMDAT
  • URL de la fuente del evento
    https://web.archive.org/web/20171014014923/http://www.titck.gov.tr/PortalAdmin/Uploads/Titck/Dynamic/sgb-2017-193.pdf
  • Notas / Alertas
    Turkish data is current through July 2017. All of the data comes from Turkey’s Drugs and Medical Devices Agency (Titck), 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 Turkey.
  • Notas adicionales en la data
Notificaciones De Seguridad De Campo acerca de Smart Flex Vascular Stent System
  • Tipo de evento
    Field Safety Notice
  • ID del evento
    2017/234 & Cordis20170216
  • Fecha
    2017-02-22
  • País del evento
    Turkey
  • Fuente del evento
    TDMDAT
  • URL de la fuente del evento
    https://web.archive.org/web/20171014002608/http://www.titck.gov.tr/PortalAdmin/Uploads/Titck/Dynamic/2017-234%20sgb.pdf
  • Notas / Alertas
    Turkish data is current through July 2017. All of the data comes from Turkey’s Drugs and Medical Devices Agency (Titck), 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 Turkey.
  • Notas adicionales en la data
Notificaciones De Seguridad De Campo acerca de Cordis Precise Pro RX Nitinol Stent System
  • Tipo de evento
    Field Safety Notice
  • ID del evento
    2016/438 & Cordis20160504_OUS
  • Fecha
    2016-05-09
  • País del evento
    Turkey
  • Fuente del evento
    TDMDAT
  • URL de la fuente del evento
    https://web.archive.org/web/20170818070553/http://titck.gov.tr/PortalAdmin/Uploads/Titck/Dynamic/2016-438-SGB.pdf
  • Notas / Alertas
    Turkish data is current through July 2017. All of the data comes from Turkey’s Drugs and Medical Devices Agency (Titck), 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 Turkey.
  • Notas adicionales en la data
Notificaciones De Seguridad De Campo acerca de Emprint Percutaneous Antenna Thermosphere Tech
  • Tipo de evento
    Field Safety Notice
  • ID del evento
    2016/201 & V26989
  • Fecha
    2016-03-04
  • País del evento
    Turkey
  • Fuente del evento
    TDMDAT
  • URL de la fuente del evento
    https://web.archive.org/web/20170817112619/http://titck.gov.tr/PortalAdmin/Uploads/Titck/Dynamic/2016_201_sgb.pdf
  • Notas / Alertas
    Turkish data is current through July 2017. All of the data comes from Turkey’s Drugs and Medical Devices Agency (Titck), 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 Turkey.
  • Notas adicionales en la data
Notificaciones De Seguridad De Campo acerca de Endo Peanut Automatic Suture Blunt Dissector 5mm
  • Tipo de evento
    Field Safety Notice
  • ID del evento
    2017/668 & FA771
  • Fecha
    2017-05-23
  • País del evento
    Turkey
  • Fuente del evento
    TDMDAT
  • URL de la fuente del evento
    https://web.archive.org/web/20171208225308/http://www.titck.gov.tr/PortalAdmin/Uploads/Titck/Dynamic/2017-668-SGB.pdf
  • Notas / Alertas
    Turkish data is current through July 2017. All of the data comes from Turkey’s Drugs and Medical Devices Agency (Titck), 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 Turkey.
  • Notas adicionales en la data
Notificaciones De Seguridad De Campo acerca de METS Modular Tumour System
  • Tipo de evento
    Field Safety Notice
  • ID del evento
    2016/1133 & SO-2016-626
  • Fecha
    2016-12-13
  • País del evento
    Turkey
  • Fuente del evento
    TDMDAT
  • URL de la fuente del evento
    https://web.archive.org/web/20170613070734/http://titck.gov.tr/PortalAdmin/Uploads/Titck/Dynamic/2016-1133%20sgb.pdf
  • Notas / Alertas
    Turkish data is current through July 2017. All of the data comes from Turkey’s Drugs and Medical Devices Agency (Titck), 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 Turkey.
  • Notas adicionales en la data
Notificaciones De Seguridad De Campo acerca de MobiCath Bi-Directional Guiding Sheath
  • Tipo de evento
    Field Safety Notice
  • ID del evento
    2017/235 & 2183787-02/07/2017-001-r
  • Fecha
    2017-02-21
  • País del evento
    Turkey
  • Fuente del evento
    TDMDAT
  • URL de la fuente del evento
    https://web.archive.org/web/20171014004732/http://www.titck.gov.tr/PortalAdmin/Uploads/Titck/Dynamic/2017-235%20sgb.pdf
  • Notas / Alertas
    Turkish data is current through July 2017. All of the data comes from Turkey’s Drugs and Medical Devices Agency (Titck), 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 Turkey.
  • Notas adicionales en la data
Notificaciones De Seguridad De Campo acerca de HemoCue HbA1c 501
  • Tipo de evento
    Field Safety Notice
  • ID del evento
    2016/207 & P-H-150311-01
  • Fecha
    2016-03-08
  • País del evento
    Turkey
  • Fuente del evento
    TDMDAT
  • URL de la fuente del evento
    https://web.archive.org/web/20170817113011/http://titck.gov.tr/PortalAdmin/Uploads/Titck/Dynamic/2016-207%20SGB.pdf
  • Notas / Alertas
    Turkish data is current through July 2017. All of the data comes from Turkey’s Drugs and Medical Devices Agency (Titck), 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 Turkey.
  • Notas adicionales en la data
Notificaciones De Seguridad De Campo acerca de IBC Aortic Punch
  • Tipo de evento
    Field Safety Notice
  • ID del evento
    2015/1212 & CAPA15-07
  • Fecha
    2015-12-24
  • País del evento
    Turkey
  • Fuente del evento
    TDMDAT
  • URL de la fuente del evento
    https://web.archive.org/web/20170817053158/http://titck.gov.tr/PortalAdmin/Uploads/Titck/Dynamic/2015-1212%20SGB.pdf
  • Notas / Alertas
    Turkish data is current through July 2017. All of the data comes from Turkey’s Drugs and Medical Devices Agency (Titck), 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 Turkey.
  • Notas adicionales en la data
Notificaciones De Seguridad De Campo acerca de Endoscopic Suction Tube
  • Tipo de evento
    Field Safety Notice
  • ID del evento
    2016/741 & 2955842-07/14/16-010-R
  • Fecha
    2016-08-09
  • País del evento
    Turkey
  • Fuente del evento
    TDMDAT
  • URL de la fuente del evento
    https://web.archive.org/web/20170817085305/http://titck.gov.tr/PortalAdmin/Uploads/Titck/Dynamic/2016_741_sgb.pdf
  • Notas / Alertas
    Turkish data is current through July 2017. All of the data comes from Turkey’s Drugs and Medical Devices Agency (Titck), 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 Turkey.
  • Notas adicionales en la data
Notificaciones De Seguridad De Campo acerca de iChem Velocity Automated Urine Chemistry System
  • Tipo de evento
    Field Safety Notice
  • ID del evento
    2016/91 & FSCA-15048
  • Fecha
    2016-01-28
  • País del evento
    Turkey
  • Fuente del evento
    TDMDAT
  • URL de la fuente del evento
    https://web.archive.org/web/20170817131519/http://titck.gov.tr/PortalAdmin/Uploads/Titck/Dynamic/2016-91%20SGB.pdf
  • Notas / Alertas
    Turkish data is current through July 2017. All of the data comes from Turkey’s Drugs and Medical Devices Agency (Titck), 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 Turkey.
  • Notas adicionales en la data
Notificaciones De Seguridad De Campo acerca de Ethicon Physiomesh Flexible Composite Mesh
  • Tipo de evento
    Field Safety Notice
  • ID del evento
    2016/486 & Ethıcon physıomesh- Gönüllü Ürün Geri Toplaması
  • Fecha
    2016-05-26
  • País del evento
    Turkey
  • Fuente del evento
    TDMDAT
  • URL de la fuente del evento
    https://web.archive.org/web/20170818091739/http://titck.gov.tr/PortalAdmin/Uploads/Titck/Dynamic/2016-486%20SGB.pdf
  • Notas / Alertas
    Turkish data is current through July 2017. All of the data comes from Turkey’s Drugs and Medical Devices Agency (Titck), 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 Turkey.
  • Notas adicionales en la data
Notificaciones De Seguridad De Campo acerca de Skintact ECG Electrode DF31L
  • Tipo de evento
    Field Safety Notice
  • ID del evento
    2016/162 & CAP-06-0062
  • Fecha
    2016-02-23
  • País del evento
    Turkey
  • Fuente del evento
    TDMDAT
  • URL de la fuente del evento
    https://web.archive.org/web/20170817153003/http://titck.gov.tr/PortalAdmin/Uploads/Titck/Dynamic/2016-162-SGB.pdf
  • Notas / Alertas
    Turkish data is current through July 2017. All of the data comes from Turkey’s Drugs and Medical Devices Agency (Titck), 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 Turkey.
  • Notas adicionales en la data
Notificaciones De Seguridad De Campo acerca de Perceval Sutureless Heart Valve
  • Tipo de evento
    Field Safety Notice
  • ID del evento
    2016/770 & FSCA_HV 2016-002
  • Fecha
    2016-08-15
  • País del evento
    Turkey
  • Fuente del evento
    TDMDAT
  • URL de la fuente del evento
    https://web.archive.org/web/20170815224606/http://titck.gov.tr/PortalAdmin/Uploads/Titck/Dynamic/2016-770-SGB.pdf
  • Notas / Alertas
    Turkish data is current through July 2017. All of the data comes from Turkey’s Drugs and Medical Devices Agency (Titck), 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 Turkey.
  • Notas adicionales en la data
Notificaciones De Seguridad De Campo acerca de SONNET Mini Battery Slot Cable
  • Tipo de evento
    Field Safety Notice
  • ID del evento
    2016/1003 & 16-002
  • Fecha
    2016-10-31
  • País del evento
    Turkey
  • Fuente del evento
    TDMDAT
  • URL de la fuente del evento
    https://web.archive.org/web/20170817123506/http://titck.gov.tr/PortalAdmin/Uploads/Titck/Dynamic/2016-1003-sgb.pdf
  • Notas / Alertas
    Turkish data is current through July 2017. All of the data comes from Turkey’s Drugs and Medical Devices Agency (Titck), 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 Turkey.
  • Notas adicionales en la data
Notificaciones De Seguridad De Campo acerca de Arctic Gel Pad
  • Tipo de evento
    Field Safety Notice
  • ID del evento
    2016/279 & FA2016-10
  • Fecha
    2016-03-23
  • País del evento
    Turkey
  • Fuente del evento
    TDMDAT
  • URL de la fuente del evento
    https://web.archive.org/web/20170817063516/http://titck.gov.tr/PortalAdmin/Uploads/Titck/Dynamic/2016_279_sgb.pdf
  • Notas / Alertas
    Turkish data is current through July 2017. All of the data comes from Turkey’s Drugs and Medical Devices Agency (Titck), 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 Turkey.
  • Notas adicionales en la data
Notificaciones De Seguridad De Campo acerca de Euphora Quick Change Balloon Dilation Catheters
  • Tipo de evento
    Field Safety Notice
  • ID del evento
    2017/728 & FA779
  • Fecha
    2017-07-17
  • País del evento
    Turkey
  • Fuente del evento
    TDMDAT
  • URL de la fuente del evento
    https://web.archive.org/web/20171208225323/http://www.titck.gov.tr/PortalAdmin/Uploads/Titck/Dynamic/2017-728-SGB.pdf
  • Notas / Alertas
    Turkish data is current through July 2017. All of the data comes from Turkey’s Drugs and Medical Devices Agency (Titck), 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 Turkey.
  • Notas adicionales en la data
Notificaciones De Seguridad De Campo acerca de DBS Lead Kit for Deep Brain Stimulation
  • Tipo de evento
    Field Safety Notice
  • ID del evento
    2017/341 & FA761
  • Fecha
    2017-03-20
  • País del evento
    Turkey
  • Fuente del evento
    TDMDAT
  • URL de la fuente del evento
    https://web.archive.org/web/20171208230006/http://www.titck.gov.tr/PortalAdmin/Uploads/Titck/Dynamic/SGB-2017-341.pdf
  • Notas / Alertas
    Turkish data is current through July 2017. All of the data comes from Turkey’s Drugs and Medical Devices Agency (Titck), 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 Turkey.
  • Notas adicionales en la data
Notificaciones De Seguridad De Campo acerca de Temporary Transvenous Pacing Lead
  • Tipo de evento
    Field Safety Notice
  • ID del evento
    2016/582 & FA721
  • Fecha
    2016-06-17
  • País del evento
    Turkey
  • Fuente del evento
    TDMDAT
  • URL de la fuente del evento
    https://web.archive.org/web/20170818063325/http://titck.gov.tr/PortalAdmin/Uploads/Titck/Dynamic/2016-582%20SGB.pdf
  • Notas / Alertas
    Turkish data is current through July 2017. All of the data comes from Turkey’s Drugs and Medical Devices Agency (Titck), 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 Turkey.
  • Notas adicionales en la data
Notificaciones De Seguridad De Campo acerca de Metalline Wound Dressings
  • Tipo de evento
    Field Safety Notice
  • ID del evento
    2016/717 & Metalline_6-2016
  • Fecha
    2016-07-25
  • País del evento
    Turkey
  • Fuente del evento
    TDMDAT
  • URL de la fuente del evento
    https://web.archive.org/web/20170815221308/http://titck.gov.tr/PortalAdmin/Uploads/Titck/Dynamic/2016-717-SGB.pdf
  • Notas / Alertas
    Turkish data is current through July 2017. All of the data comes from Turkey’s Drugs and Medical Devices Agency (Titck), 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 Turkey.
  • Notas adicionales en la data
Notificaciones De Seguridad De Campo acerca de SynchroMed Implantable Infusion Pump
  • Tipo de evento
    Field Safety Notice
  • ID del evento
    2016/704 & FA696
  • Fecha
    2016-07-25
  • País del evento
    Turkey
  • Fuente del evento
    TDMDAT
  • URL de la fuente del evento
    https://web.archive.org/web/20170815182026/http://titck.gov.tr/PortalAdmin/Uploads/Titck/Dynamic/2016-704%20SGB.pdf
  • Notas / Alertas
    Turkish data is current through July 2017. All of the data comes from Turkey’s Drugs and Medical Devices Agency (Titck), 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 Turkey.
  • Notas adicionales en la data
Notificaciones De Seguridad De Campo acerca de Endurant / Endurant II Forked Stent Graft Systems
  • Tipo de evento
    Field Safety Notice
  • ID del evento
    2017/266 & FA758
  • Fecha
    2017-03-02
  • País del evento
    Turkey
  • Fuente del evento
    TDMDAT
  • URL de la fuente del evento
    https://web.archive.org/web/20171014002232/http://www.titck.gov.tr/PortalAdmin/Uploads/Titck/Dynamic/2017-266-SGB.pdf
  • Notas / Alertas
    Turkish data is current through July 2017. All of the data comes from Turkey’s Drugs and Medical Devices Agency (Titck), 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 Turkey.
  • Notas adicionales en la data
Notificaciones De Seguridad De Campo acerca de DLP 20-inch extension line adapters
  • Tipo de evento
    Field Safety Notice
  • ID del evento
    2017/726 & FA778
  • Fecha
    2017-06-28
  • País del evento
    Turkey
  • Fuente del evento
    TDMDAT
  • URL de la fuente del evento
    https://web.archive.org/web/20171208225319/http://www.titck.gov.tr/PortalAdmin/Uploads/Titck/Dynamic/2017-726-SGB.pdf
  • Notas / Alertas
    Turkish data is current through July 2017. All of the data comes from Turkey’s Drugs and Medical Devices Agency (Titck), 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 Turkey.
  • Notas adicionales en la data
Notificaciones De Seguridad De Campo acerca de Pipeline Embolization Device, Alligator Retrieval ...
  • Tipo de evento
    Field Safety Notice
  • ID del evento
    2016/928 & FA740
  • Fecha
    2016-10-11
  • País del evento
    Turkey
  • Fuente del evento
    TDMDAT
  • URL de la fuente del evento
    https://web.archive.org/web/20170817155617/http://titck.gov.tr/PortalAdmin/Uploads/Titck/Dynamic/2016_%20928%20SGB.pdf
  • Notas / Alertas
    Turkish data is current through July 2017. All of the data comes from Turkey’s Drugs and Medical Devices Agency (Titck), 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 Turkey.
  • Notas adicionales en la data
Notificaciones De Seguridad De Campo acerca de PHIL Non-Adhesive Fluid System
  • Tipo de evento
    Field Safety Notice
  • ID del evento
    2016/641 & NA
  • Fecha
    2016-07-01
  • País del evento
    Turkey
  • Fuente del evento
    TDMDAT
  • URL de la fuente del evento
    https://web.archive.org/web/20170818074943/http://titck.gov.tr/PortalAdmin/Uploads/Titck/Dynamic/2016-641%20sgb.pdf
  • Notas / Alertas
    Turkish data is current through July 2017. All of the data comes from Turkey’s Drugs and Medical Devices Agency (Titck), 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 Turkey.
  • Notas adicionales en la data
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Acerca de la base de datos

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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.