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Mode Liste Mode Grille
  • Dispositif médical 1003
  • Fabricant 257
  • Événement 124969
  • Implant 20
Avis De Sécurité sur Bigliani/Flatow® Fukuda Retractors
  • Type d'événement
    Field Safety Notice
  • ID de l'événement
    03361/13
  • Date
    2013-06-21
  • Pays de l'événement
    Germany
  • Source de l'événement
    BAM
  • URL de la source de l'événement
    https://www.bfarm.de/SharedDocs/Kundeninfos/EN/06/2013/03361-13_kundeninfo_en.html
  • Notes / Alertes
    German data is current through October 2018. All of the data comes from Bundesinstitut für Arzneimittel und Medizinprodukte, 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 Germany.
  • Notes supplémentaires dans les données
Avis De Sécurité sur NexGen® CR Micro Implants and Provisionals
  • Type d'événement
    Field Safety Notice
  • ID de l'événement
    03776/13
  • Date
    2013-07-10
  • Pays de l'événement
    Germany
  • Source de l'événement
    BAM
  • URL de la source de l'événement
    https://www.bfarm.de/SharedDocs/Kundeninfos/EN/11/2013/03776-13_kundeninfo_en.html
  • Notes / Alertes
    German data is current through October 2018. All of the data comes from Bundesinstitut für Arzneimittel und Medizinprodukte, 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 Germany.
  • Notes supplémentaires dans les données
Avis De Sécurité sur Trabecular Metal Reverse Glenosphere Helmet
  • Type d'événement
    Field Safety Notice
  • ID de l'événement
    04557/13
  • Date
    2013-08-14
  • Pays de l'événement
    Germany
  • Source de l'événement
    BAM
  • URL de la source de l'événement
    https://www.bfarm.de/SharedDocs/Kundeninfos/EN/06/2013/4557-13_Kundeninfo_en.html
  • Notes / Alertes
    German data is current through October 2018. All of the data comes from Bundesinstitut für Arzneimittel und Medizinprodukte, 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 Germany.
  • Notes supplémentaires dans les données
Avis De Sécurité sur Trabecular Metal™ Reverse Glenosphere Distractor
  • Type d'événement
    Field Safety Notice
  • ID de l'événement
    05052/13
  • Date
    2013-09-02
  • Pays de l'événement
    Germany
  • Source de l'événement
    BAM
  • URL de la source de l'événement
    https://www.bfarm.de/SharedDocs/Kundeninfos/EN/06/2013/5052-13_Kundeninfo_en.html
  • Notes / Alertes
    German data is current through October 2018. All of the data comes from Bundesinstitut für Arzneimittel und Medizinprodukte, 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 Germany.
  • Notes supplémentaires dans les données
Avis De Sécurité sur highly polished implants, that were packaged in a LDPE bag
  • Type d'événement
    Field Safety Notice
  • ID de l'événement
    05280/13
  • Date
    2013-09-23
  • Pays de l'événement
    Germany
  • Source de l'événement
    BAM
  • URL de la source de l'événement
    https://www.bfarm.de/SharedDocs/Kundeninfos/EN/11/2013/05280-13_kundeninfo_en.html
  • Notes / Alertes
    German data is current through October 2018. All of the data comes from Bundesinstitut für Arzneimittel und Medizinprodukte, 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 Germany.
  • Notes supplémentaires dans les données
Avis De Sécurité sur (phase 2) of the Trabecular Metal Reverse Glenosphere Helmets
  • Type d'événement
    Field Safety Notice
  • ID de l'événement
    04557/13
  • Date
    2013-11-28
  • Pays de l'événement
    Germany
  • Source de l'événement
    BAM
  • URL de la source de l'événement
    https://www.bfarm.de/SharedDocs/Kundeninfos/EN/06/2013/04557-13_kundeninfo_en.html
  • Notes / Alertes
    German data is current through October 2018. All of the data comes from Bundesinstitut für Arzneimittel und Medizinprodukte, 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 Germany.
  • Notes supplémentaires dans les données
Avis De Sécurité sur Etest Colistin CO 256 WW
  • Type d'événement
    Field Safety Notice
  • ID de l'événement
    600:41/01-146/16/08_22
  • Date
    2016-08-03
  • Pays de l'événement
    Singapore
  • Source de l'événement
    HSA
  • URL de la source de l'événement
    https://www.hsa.gov.sg/announcements
  • Notes / Alertes
    Data from Singapore is current through September 2018. All of the data comes from the Health Sciences Authority (HSA), 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 Singapore.
  • Notes supplémentaires dans les données
    bioMérieux SA
Avis De Sécurité sur several Polyethylene Implants
  • Type d'événement
    Field Safety Notice
  • ID de l'événement
    01606/14
  • Date
    2014-03-31
  • Pays de l'événement
    Germany
  • Source de l'événement
    BAM
  • URL de la source de l'événement
    https://www.bfarm.de/SharedDocs/Kundeninfos/EN/11/2014/01606-14_kundeninfo_en.html
  • Notes / Alertes
    German data is current through October 2018. All of the data comes from Bundesinstitut für Arzneimittel und Medizinprodukte, 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 Germany.
  • Notes supplémentaires dans les données
Avis De Sécurité sur the Persona Stemmed 5 Degree Cemented Tibia, various sizes
  • Type d'événement
    Field Safety Notice
  • ID de l'événement
    07321/14
  • Date
    2014-11-07
  • Pays de l'événement
    Germany
  • Source de l'événement
    BAM
  • URL de la source de l'événement
    https://www.bfarm.de/SharedDocs/Kundeninfos/EN/11/2014/07321-14_kundeninfo_en.html
  • Notes / Alertes
    German data is current through October 2018. All of the data comes from Bundesinstitut für Arzneimittel und Medizinprodukte, 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 Germany.
  • Notes supplémentaires dans les données
Avis De Sécurité sur the PF Stem lateralized cemented size 8 and PF Stem Standard cemented Size 7
  • Type d'événement
    Field Safety Notice
  • ID de l'événement
    07959/14
  • Date
    2014-12-10
  • Pays de l'événement
    Germany
  • Source de l'événement
    BAM
  • URL de la source de l'événement
    https://www.bfarm.de/SharedDocs/Kundeninfos/EN/11/2014/07959-14_kundeninfo_en.html
  • Notes / Alertes
    German data is current through October 2018. All of the data comes from Bundesinstitut für Arzneimittel und Medizinprodukte, 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 Germany.
  • Notes supplémentaires dans les données
Avis De Sécurité sur Various Sterile-Packaged Femoral Heads and Tapers
  • Type d'événement
    Field Safety Notice
  • ID de l'événement
    00073/15
  • Date
    2015-02-02
  • Pays de l'événement
    Germany
  • Source de l'événement
    BAM
  • URL de la source de l'événement
    https://www.bfarm.de/SharedDocs/Kundeninfos/EN/11/2015/00073-15_kundeninfo_en.html
  • Notes / Alertes
    German data is current through October 2018. All of the data comes from Bundesinstitut für Arzneimittel und Medizinprodukte, 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 Germany.
  • Notes supplémentaires dans les données
Avis De Sécurité sur the Anatomical Shoulder Handle for Rasp
  • Type d'événement
    Field Safety Notice
  • ID de l'événement
    01789/15
  • Date
    2015-04-07
  • Pays de l'événement
    Germany
  • Source de l'événement
    BAM
  • URL de la source de l'événement
    https://www.bfarm.de/SharedDocs/Kundeninfos/EN/06/2015/01789-15_kundeninfo_en.html
  • Notes / Alertes
    German data is current through October 2018. All of the data comes from Bundesinstitut für Arzneimittel und Medizinprodukte, 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 Germany.
  • Notes supplémentaires dans les données
Avis De Sécurité sur Persona Cemented Tibia Drill Bracket
  • Type d'événement
    Field Safety Notice
  • ID de l'événement
    02382/15
  • Date
    2015-04-23
  • Pays de l'événement
    Germany
  • Source de l'événement
    BAM
  • URL de la source de l'événement
    https://www.bfarm.de/SharedDocs/Kundeninfos/EN/06/2015/02382-15_kundeninfo_en.html
  • Notes / Alertes
    German data is current through October 2018. All of the data comes from Bundesinstitut für Arzneimittel und Medizinprodukte, 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 Germany.
  • Notes supplémentaires dans les données
Avis De Sécurité sur NexGen CRA/LCCK/RHK 5 mm Distal Femoral Augment, Size F
  • Type d'événement
    Field Safety Notice
  • ID de l'événement
    02373/15
  • Date
    2015-04-23
  • Pays de l'événement
    Germany
  • Source de l'événement
    BAM
  • URL de la source de l'événement
    https://www.bfarm.de/SharedDocs/Kundeninfos/EN/11/2015/02373-15_kundeninfo_en.html
  • Notes / Alertes
    German data is current through October 2018. All of the data comes from Bundesinstitut für Arzneimittel und Medizinprodukte, 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 Germany.
  • Notes supplémentaires dans les données
Avis De Sécurité sur Muller Hinton 2 agar + 5% sheep blood
  • Type d'événement
    Field Safety Notice
  • ID de l'événement
    600:41/01-146/16/09_58
  • Date
    2016-08-29
  • Pays de l'événement
    Singapore
  • Source de l'événement
    HSA
  • URL de la source de l'événement
    https://www.hsa.gov.sg/announcements
  • Notes / Alertes
    Data from Singapore is current through September 2018. All of the data comes from the Health Sciences Authority (HSA), 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 Singapore.
  • Notes supplémentaires dans les données
    BioMérieux SA
Avis De Sécurité sur guide wires labeled with a 10-year expiration date
  • Type d'événement
    Field Safety Notice
  • ID de l'événement
    06637/15
  • Date
    2015-10-09
  • Pays de l'événement
    Germany
  • Source de l'événement
    BAM
  • URL de la source de l'événement
    https://www.bfarm.de/SharedDocs/Kundeninfos/EN/06/2015/06637-15_kundeninfo_en.html
  • Notes / Alertes
    German data is current through October 2018. All of the data comes from Bundesinstitut für Arzneimittel und Medizinprodukte, 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 Germany.
  • Notes supplémentaires dans les données
Avis De Sécurité sur Persona EM Proximal Tube and Persona EM Distal Rod
  • Type d'événement
    Field Safety Notice
  • ID de l'événement
    09338/15
  • Date
    2015-12-14
  • Pays de l'événement
    Germany
  • Source de l'événement
    BAM
  • URL de la source de l'événement
    https://www.bfarm.de/SharedDocs/Kundeninfos/EN/06/2015/09338-15_kundeninfo_en.html
  • Notes / Alertes
    German data is current through October 2018. All of the data comes from Bundesinstitut für Arzneimittel und Medizinprodukte, 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 Germany.
  • Notes supplémentaires dans les données
Avis De Sécurité sur several Hip, Knee and Shoulder products with high polished surface packaged ...
  • Type d'événement
    Field Safety Notice
  • ID de l'événement
    00646/16
  • Date
    2016-02-17
  • Pays de l'événement
    Germany
  • Source de l'événement
    BAM
  • URL de la source de l'événement
    https://www.bfarm.de/SharedDocs/Kundeninfos/EN/11/2016/00646-16_kundeninfo_en.html
  • Notes / Alertes
    German data is current through October 2018. All of the data comes from Bundesinstitut für Arzneimittel und Medizinprodukte, 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 Germany.
  • Notes supplémentaires dans les données
Avis De Sécurité sur several Hip, Knee and Shoulder products with high polished surface packaged ...
  • Type d'événement
    Field Safety Notice
  • ID de l'événement
    00645/16
  • Date
    2016-02-17
  • Pays de l'événement
    Germany
  • Source de l'événement
    BAM
  • URL de la source de l'événement
    https://www.bfarm.de/SharedDocs/Kundeninfos/EN/11/2016/00645-16_kundeninfo_en.html
  • Notes / Alertes
    German data is current through October 2018. All of the data comes from Bundesinstitut für Arzneimittel und Medizinprodukte, 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 Germany.
  • Notes supplémentaires dans les données
Avis De Sécurité sur DVR ePAKs
  • Type d'événement
    Field Safety Notice
  • ID de l'événement
    01176/16
  • Date
    2016-02-18
  • Pays de l'événement
    Germany
  • Source de l'événement
    BAM
  • URL de la source de l'événement
    https://www.bfarm.de/SharedDocs/Kundeninfos/EN/11/2016/01176-16_kundeninfo_en.html
  • Notes / Alertes
    German data is current through October 2018. All of the data comes from Bundesinstitut für Arzneimittel und Medizinprodukte, 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 Germany.
  • Notes supplémentaires dans les données
Avis De Sécurité sur Instinct Java System Instruments, all lot numbers / Universal Clamp System I...
  • Type d'événement
    Field Safety Notice
  • ID de l'événement
    01836/16
  • Date
    2016-04-01
  • Pays de l'événement
    Germany
  • Source de l'événement
    BAM
  • URL de la source de l'événement
    https://www.bfarm.de/SharedDocs/Kundeninfos/EN/06/2016/01836-16_kundeninfo_en.html
  • Notes / Alertes
    German data is current through October 2018. All of the data comes from Bundesinstitut für Arzneimittel und Medizinprodukte, 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 Germany.
  • Notes supplémentaires dans les données
Avis De Sécurité sur M2a 38mm Acetabular System
  • Type d'événement
    Field Safety Notice
  • ID de l'événement
    03156/16
  • Date
    2016-04-19
  • Pays de l'événement
    Germany
  • Source de l'événement
    BAM
  • URL de la source de l'événement
    https://www.bfarm.de/SharedDocs/Kundeninfos/EN/11/2016/03156-16_kundeninfo_en.html
  • Notes / Alertes
    German data is current through October 2018. All of the data comes from Bundesinstitut für Arzneimittel und Medizinprodukte, 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 Germany.
  • Notes supplémentaires dans les données
Avis De Sécurité sur various sports medicine and trauma products
  • Type d'événement
    Field Safety Notice
  • ID de l'événement
    03344/16
  • Date
    2016-04-27
  • Pays de l'événement
    Germany
  • Source de l'événement
    BAM
  • URL de la source de l'événement
    https://www.bfarm.de/SharedDocs/Kundeninfos/EN/11/2016/03344-16_kundeninfo_en.html
  • Notes / Alertes
    German data is current through October 2018. All of the data comes from Bundesinstitut für Arzneimittel und Medizinprodukte, 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 Germany.
  • Notes supplémentaires dans les données
Avis De Sécurité sur Normed Fender Titanium Plates
  • Type d'événement
    Field Safety Notice
  • ID de l'événement
    03733/16
  • Date
    2016-05-10
  • Pays de l'événement
    Germany
  • Source de l'événement
    BAM
  • URL de la source de l'événement
    https://www.bfarm.de/SharedDocs/Kundeninfos/EN/11/2016/03733-16_kundeninfo_en.html
  • Notes / Alertes
    German data is current through October 2018. All of the data comes from Bundesinstitut für Arzneimittel und Medizinprodukte, 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 Germany.
  • Notes supplémentaires dans les données
Avis De Sécurité sur various sterile-packaged knee and hip implants
  • Type d'événement
    Field Safety Notice
  • ID de l'événement
    03908/16
  • Date
    2016-05-10
  • Pays de l'événement
    Germany
  • Source de l'événement
    BAM
  • URL de la source de l'événement
    https://www.bfarm.de/SharedDocs/Kundeninfos/EN/11/2016/03908-16_kundeninfo_en.html
  • Notes / Alertes
    German data is current through October 2018. All of the data comes from Bundesinstitut für Arzneimittel und Medizinprodukte, 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 Germany.
  • Notes supplémentaires dans les données
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Explorez plus de 120,000 rappels, alertes et avis de sécurité concernant les dispositifs médicaux, ainsi que leurs liens avec leurs fabricants.

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