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Mode Liste Mode Grille
  • Dispositif médical 1003
  • Fabricant 257
  • Événement 124969
  • Implant 20
Avis De Sécurité sur Cisco ASA 5506-X Network Firewall
  • Type d'événement
    Field Safety Notice
  • Numéro de l'événement
    2017112281
  • Date
    2017-11-15
  • Pays de l'événement
    Denmark
  • Source de l'événement
    DMA
  • URL de la source de l'événement
    https://laegemiddelstyrelsen.dk/da/udstyr/sikkerhedsmeddelelser/2017/11/cisco-asa-5506-x-network-firewall/
  • Notes / Alertes
    Danish data is current through March 2019. All of the data comes from the Danish Medicines Agency, 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 data from the U.S. and Denmark.
  • Notes supplémentaires dans les données
Avis De Sécurité sur MobileDiagnost wDR
  • Type d'événement
    Field Safety Notice
  • Numéro de l'événement
    2013103562
  • Date
    2013-10-31
  • Pays de l'événement
    Denmark
  • Source de l'événement
    DMA
  • URL de la source de l'événement
    https://laegemiddelstyrelsen.dk/da/udstyr/sikkerhedsmeddelelser/2013/mobilediagnost-wdr-oktober-2013/
  • Notes / Alertes
    Danish data is current through March 2019. All of the data comes from the Danish Medicines Agency, 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 data from the U.S. and Denmark.
  • Notes supplémentaires dans les données
Avis De Sécurité sur gemini pet/ct-system
  • Type d'événement
    Field Safety Notice
  • Numéro de l'événement
    2015072906
  • Date
    2015-07-23
  • Pays de l'événement
    Denmark
  • Source de l'événement
    DMA
  • URL de la source de l'événement
    https://laegemiddelstyrelsen.dk/da/udstyr/sikkerhedsmeddelelser/2015/07/gemini-petct-systemer/
  • Notes / Alertes
    Danish data is current through March 2019. All of the data comes from the Danish Medicines Agency, 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 data from the U.S. and Denmark.
  • Notes supplémentaires dans les données
Avis De Sécurité sur extended brilliance workstation with softwareversion 4.0.2, 4.5.2, 4.5.3
  • Type d'événement
    Field Safety Notice
  • Numéro de l'événement
    LMST-2012103461
  • Date
    2012-10-25
  • Pays de l'événement
    Denmark
  • Source de l'événement
    DMA
  • URL de la source de l'événement
    https://laegemiddelstyrelsen.dk/da/udstyr/sikkerhedsmeddelelser/2012/extended-brilliance-workstation-ebw-med-softwareversion-402,-452,-453/
  • Notes / Alertes
    Danish data is current through March 2019. All of the data comes from the Danish Medicines Agency, 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 data from the U.S. and Denmark.
  • Notes supplémentaires dans les données
Avis De Sécurité sur HeartStart MRx Defibrillator/Monitor
  • Type d'événement
    Field Safety Notice
  • Numéro de l'événement
    2013063346
  • Date
    2013-06-25
  • Pays de l'événement
    Denmark
  • Source de l'événement
    DMA
  • URL de la source de l'événement
    https://laegemiddelstyrelsen.dk/da/udstyr/sikkerhedsmeddelelser/2013/heartstart-mrx-defibrillatormonitor/
  • Notes / Alertes
    Danish data is current through March 2019. All of the data comes from the Danish Medicines Agency, 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 data from the U.S. and Denmark.
  • Notes supplémentaires dans les données
Avis De Sécurité sur brilliance 6, 10, 16, 40, 64 and brilliance ct big bore
  • Type d'événement
    Field Safety Notice
  • Numéro de l'événement
    LMST-2012083511
  • Date
    2012-08-28
  • Pays de l'événement
    Denmark
  • Source de l'événement
    DMA
  • URL de la source de l'événement
    https://laegemiddelstyrelsen.dk/da/udstyr/sikkerhedsmeddelelser/2012/brilliance-6,-10,-16,-40,-64-og-brilliance-ct-big-bore/
  • Notes / Alertes
    Danish data is current through March 2019. All of the data comes from the Danish Medicines Agency, 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 data from the U.S. and Denmark.
  • Notes supplémentaires dans les données
Avis De Sécurité sur IntelliSpace Portal version 4.0.2
  • Type d'événement
    Field Safety Notice
  • Numéro de l'événement
    2013031377
  • Date
    2013-03-11
  • Pays de l'événement
    Denmark
  • Source de l'événement
    DMA
  • URL de la source de l'événement
    https://laegemiddelstyrelsen.dk/da/udstyr/sikkerhedsmeddelelser/2013/intellispace-portal/
  • Notes / Alertes
    Danish data is current through March 2019. All of the data comes from the Danish Medicines Agency, 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 data from the U.S. and Denmark.
  • Notes supplémentaires dans les données
Avis De Sécurité sur brilliance br64, ingenuity ct, ingenuity core and ingenuity core128
  • Type d'événement
    Field Safety Notice
  • Numéro de l'événement
    2017100822
  • Date
    2017-10-05
  • Pays de l'événement
    Denmark
  • Source de l'événement
    DMA
  • URL de la source de l'événement
    https://laegemiddelstyrelsen.dk/da/udstyr/sikkerhedsmeddelelser/2017/10/brilliance-br64,-ingenuity-ct,-ingenuity-core-og-ingenuity-core128/
  • Notes / Alertes
    Danish data is current through March 2019. All of the data comes from the Danish Medicines Agency, 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 data from the U.S. and Denmark.
  • Notes supplémentaires dans les données
Avis De Sécurité sur MultiDiagnost Eleva FD R5.1.x
  • Type d'événement
    Field Safety Notice
  • Numéro de l'événement
    LMST-2012092967
  • Date
    2012-09-25
  • Pays de l'événement
    Denmark
  • Source de l'événement
    DMA
  • URL de la source de l'événement
    https://laegemiddelstyrelsen.dk/da/udstyr/sikkerhedsmeddelelser/2012/multidiagnost-eleva-fd-r51x/
  • Notes / Alertes
    Danish data is current through March 2019. All of the data comes from the Danish Medicines Agency, 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 data from the U.S. and Denmark.
  • Notes supplémentaires dans les données
Avis De Sécurité sur digitaldiagnost patient cart serial number 00 000 00 to 09 000 543
  • Type d'événement
    Field Safety Notice
  • Numéro de l'événement
    LMST-2012101002
  • Date
    2012-10-08
  • Pays de l'événement
    Denmark
  • Source de l'événement
    DMA
  • URL de la source de l'événement
    https://laegemiddelstyrelsen.dk/da/udstyr/sikkerhedsmeddelelser/2012/digitaldiagnost-patientvognen-serienummer-00-000-00-til-09-000-543/
  • Notes / Alertes
    Danish data is current through March 2019. All of the data comes from the Danish Medicines Agency, 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 data from the U.S. and Denmark.
  • Notes supplémentaires dans les données
Avis De Sécurité sur HeartStart MRx with Wireless Link Upgrade
  • Type d'événement
    Field Safety Notice
  • Numéro de l'événement
    2014043255
  • Date
    2014-04-29
  • Pays de l'événement
    Denmark
  • Source de l'événement
    DMA
  • URL de la source de l'événement
    https://laegemiddelstyrelsen.dk/da/udstyr/sikkerhedsmeddelelser/2014/heartstart-mrx-with-wireless-link-upgrade-/
  • Notes / Alertes
    Danish data is current through March 2019. All of the data comes from the Danish Medicines Agency, 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 data from the U.S. and Denmark.
  • Notes supplémentaires dans les données
Avis De Sécurité sur Philips IntelliVue Patient Monitors
  • Type d'événement
    Field Safety Notice
  • Numéro de l'événement
    LMST-2012022068
  • Date
    2012-02-21
  • Pays de l'événement
    Denmark
  • Source de l'événement
    DMA
  • URL de la source de l'événement
    https://laegemiddelstyrelsen.dk/da/udstyr/sikkerhedsmeddelelser/2012/philips-intellivue-patient-skaerme/
  • Notes / Alertes
    Danish data is current through March 2019. All of the data comes from the Danish Medicines Agency, 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 data from the U.S. and Denmark.
  • Notes supplémentaires dans les données
Avis De Sécurité sur brilliance br64 and ingenuity ct / core / core128
  • Type d'événement
    Field Safety Notice
  • Numéro de l'événement
    2016092619
  • Date
    2016-09-20
  • Pays de l'événement
    Denmark
  • Source de l'événement
    DMA
  • URL de la source de l'événement
    https://laegemiddelstyrelsen.dk/da/udstyr/sikkerhedsmeddelelser/2016/09/philips-brilliance-64-og-ingenuity-ctcorecore128/
  • Notes / Alertes
    Danish data is current through March 2019. All of the data comes from the Danish Medicines Agency, 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 data from the U.S. and Denmark.
  • Notes supplémentaires dans les données
Avis De Sécurité sur Philips HeartStart XL+-defibrillator/monitor
  • Type d'événement
    Field Safety Notice
  • Numéro de l'événement
    2014043522
  • Date
    2014-04-29
  • Pays de l'événement
    Denmark
  • Source de l'événement
    DMA
  • URL de la source de l'événement
    https://laegemiddelstyrelsen.dk/da/udstyr/sikkerhedsmeddelelser/2014/philips-heartstart-xl-defibrillatormonitor/
  • Notes / Alertes
    Danish data is current through March 2019. All of the data comes from the Danish Medicines Agency, 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 data from the U.S. and Denmark.
  • Notes supplémentaires dans les données
Avis De Sécurité sur precedence imaging system and skylight gamma camera
  • Type d'événement
    Field Safety Notice
  • Numéro de l'événement
    LMST-2012032548
  • Date
    2012-03-20
  • Pays de l'événement
    Denmark
  • Source de l'événement
    DMA
  • URL de la source de l'événement
    https://laegemiddelstyrelsen.dk/da/udstyr/sikkerhedsmeddelelser/2012/precedence-og-skylight-spect-systemer/
  • Notes / Alertes
    Danish data is current through March 2019. All of the data comes from the Danish Medicines Agency, 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 data from the U.S. and Denmark.
  • Notes supplémentaires dans les données
Avis De Sécurité sur AFFINITI 50
  • Type d'événement
    Field Safety Notice
  • Numéro de l'événement
    2015072885
  • Date
    2015-07-23
  • Pays de l'événement
    Denmark
  • Source de l'événement
    DMA
  • URL de la source de l'événement
    https://laegemiddelstyrelsen.dk/da/udstyr/sikkerhedsmeddelelser/2015/07/affiniti-50/
  • Notes / Alertes
    Danish data is current through March 2019. All of the data comes from the Danish Medicines Agency, 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 data from the U.S. and Denmark.
  • Notes supplémentaires dans les données
Avis De Sécurité sur xper flex cardio patient monitoring system
  • Type d'événement
    Field Safety Notice
  • Numéro de l'événement
    2019020198
  • Date
    2019-02-01
  • Pays de l'événement
    Denmark
  • Source de l'événement
    DMA
  • URL de la source de l'événement
    https://laegemiddelstyrelsen.dk/da/udstyr/sikkerhedsmeddelelser/2019/2/xper-flex-cardio-patientmonitoreringssystemet/
  • Notes / Alertes
    Danish data is current through March 2019. All of the data comes from the Danish Medicines Agency, 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 data from the U.S. and Denmark.
  • Notes supplémentaires dans les données
Avis De Sécurité sur Philips HeartStart FRx AED, Philips HS1 (Onsite) AED, Philips HS1 (Home) AED
  • Type d'événement
    Field Safety Notice
  • Numéro de l'événement
    2018032050
  • Date
    2018-03-13
  • Pays de l'événement
    Denmark
  • Source de l'événement
    DMA
  • URL de la source de l'événement
    https://laegemiddelstyrelsen.dk/da/udstyr/sikkerhedsmeddelelser/2018/03/philips-heartstart-frx-aed,-philips-hs1-onsite-aed,-philips-hs1-home-aed/
  • Notes / Alertes
    Danish data is current through March 2019. All of the data comes from the Danish Medicines Agency, 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 data from the U.S. and Denmark.
  • Notes supplémentaires dans les données
Avis De Sécurité sur CPR Meter w/Q-CPR® Technology
  • Type d'événement
    Field Safety Notice
  • Numéro de l'événement
    2018023837
  • Date
    2018-02-23
  • Pays de l'événement
    Denmark
  • Source de l'événement
    DMA
  • URL de la source de l'événement
    https://laegemiddelstyrelsen.dk/da/udstyr/sikkerhedsmeddelelser/2018/02/cpr-meter-wq-cpr-technology/
  • Notes / Alertes
    Danish data is current through March 2019. All of the data comes from the Danish Medicines Agency, 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 data from the U.S. and Denmark.
  • Notes supplémentaires dans les données
Avis De Sécurité sur xper flex cardio patient monitoring system
  • Type d'événement
    Field Safety Notice
  • Numéro de l'événement
    2016011842
  • Date
    2016-01-14
  • Pays de l'événement
    Denmark
  • Source de l'événement
    DMA
  • URL de la source de l'événement
    https://laegemiddelstyrelsen.dk/da/udstyr/sikkerhedsmeddelelser/2016/01/xper-flex-cardio-patientmonitoreringssystem/
  • Notes / Alertes
    Danish data is current through March 2019. All of the data comes from the Danish Medicines Agency, 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 data from the U.S. and Denmark.
  • Notes supplémentaires dans les données
Avis De Sécurité sur Ingenia, Intera, Achieva and Multiva MR Systems
  • Type d'événement
    Field Safety Notice
  • Numéro de l'événement
    2014060033
  • Date
    2014-06-03
  • Pays de l'événement
    Denmark
  • Source de l'événement
    DMA
  • URL de la source de l'événement
    https://laegemiddelstyrelsen.dk/da/udstyr/sikkerhedsmeddelelser/2014/ingenia,-intera,-achieva-and-multiva-mr-systems/
  • Notes / Alertes
    Danish data is current through March 2019. All of the data comes from the Danish Medicines Agency, 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 data from the U.S. and Denmark.
  • Notes supplémentaires dans les données
Avis De Sécurité sur IntelliVue MX40 Patient Monitor
  • Type d'événement
    Field Safety Notice
  • Numéro de l'événement
    2018064408
  • Date
    2018-06-29
  • Pays de l'événement
    Denmark
  • Source de l'événement
    DMA
  • URL de la source de l'événement
    https://laegemiddelstyrelsen.dk/da/udstyr/sikkerhedsmeddelelser/2018/06/intellivue-mx40-patient-monitor/
  • Notes / Alertes
    Danish data is current through March 2019. All of the data comes from the Danish Medicines Agency, 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 data from the U.S. and Denmark.
  • Notes supplémentaires dans les données
Avis De Sécurité sur QLAB
  • Type d'événement
    Field Safety Notice
  • Numéro de l'événement
    2014114911
  • Date
    2014-11-28
  • Pays de l'événement
    Denmark
  • Source de l'événement
    DMA
  • URL de la source de l'événement
    https://laegemiddelstyrelsen.dk/da/udstyr/sikkerhedsmeddelelser/2014/philips-ultrasound-qlab/
  • Notes / Alertes
    Danish data is current through March 2019. All of the data comes from the Danish Medicines Agency, 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 data from the U.S. and Denmark.
  • Notes supplémentaires dans les données
Avis De Sécurité sur Philips SureSigns VSi / SureSigns VS2+
  • Type d'événement
    Field Safety Notice
  • Numéro de l'événement
    2018024271
  • Date
    2018-02-27
  • Pays de l'événement
    Denmark
  • Source de l'événement
    DMA
  • URL de la source de l'événement
    https://laegemiddelstyrelsen.dk/da/udstyr/sikkerhedsmeddelelser/2018/02/philips-suresigns-vsi-suresigns-vs2/
  • Notes / Alertes
    Danish data is current through March 2019. All of the data comes from the Danish Medicines Agency, 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 data from the U.S. and Denmark.
  • Notes supplémentaires dans les données
Avis De Sécurité sur Philips Expression IP5 Informationsportal
  • Type d'événement
    Field Safety Notice
  • Numéro de l'événement
    2014072893
  • Date
    2014-07-29
  • Pays de l'événement
    Denmark
  • Source de l'événement
    DMA
  • URL de la source de l'événement
    https://laegemiddelstyrelsen.dk/da/udstyr/sikkerhedsmeddelelser/2014/philips-expression-ip5-informationsportal/
  • Notes / Alertes
    Danish data is current through March 2019. All of the data comes from the Danish Medicines Agency, 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 data from the U.S. and Denmark.
  • Notes supplémentaires dans les données
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