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Vista de la lista Vista de las tarjetas
  • Dispositivo 145
  • Fabricante 78
  • Evento 124969
  • Implante 0
Notificaciones De Seguridad De Campo acerca de aquarius rca hemofiltration system
  • Tipo de evento
    Field Safety Notice
  • ID del evento
    2197
  • Fecha
    2011-11-16
  • País del evento
    Poland
  • Fuente del evento
    ORMPMDBP
  • URL de la fuente del evento
    http://www.urpl.gov.pl/pl/notatka-bezpiecze%C5%84stwa-firmy-nikkiso-dotycz%C4%85ca-systemu-hemofiltracji-aquarius-rca
  • Notas / Alertas
    Polish data is current through November 2018. All of the data comes from the Office for Registration of Medicinal Products, Medical Devices and Biocidal Products, 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 Poland.
  • Notas adicionales en la data
  • Acción
    NIKKISO safety note regarding the AQUARIUS RCA hemofiltration system.
Notificaciones De Seguridad De Campo acerca de dialysate cleaning filters, type ef-02d
  • Tipo de evento
    Field Safety Notice
  • ID del evento
    1612
  • Fecha
    2010-11-29
  • País del evento
    Poland
  • Fuente del evento
    ORMPMDBP
  • URL de la fuente del evento
    http://www.urpl.gov.pl/pl/komunikat-firmy-nikkiso-dotycz%C4%85cy-filtr%C3%B3w-do-czyszczenia-dializatu-typu-ef-02d
  • Notas / Alertas
    Polish data is current through November 2018. All of the data comes from the Office for Registration of Medicinal Products, Medical Devices and Biocidal Products, 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 Poland.
  • Notas adicionales en la data
  • Acción
    NIKKISO's message regarding dialysate cleaning filters, type EF-02D
Notificaciones De Seguridad De Campo acerca de umbilical iron clamps, series number 20161026
  • Tipo de evento
    Field Safety Notice
  • ID del evento
    205
  • Fecha
    2017-07-12
  • País del evento
    Poland
  • Fuente del evento
    ORMPMDBP
  • URL de la fuente del evento
    http://www.urpl.gov.pl/pl/notatka-bezpiecze%C5%84stwa-firmy-ningbo-greetmed-medica-dotycz%C4%85ca-wycofania-z-obrotu-i-z-u%C5%BCywania
  • Notas / Alertas
    Polish data is current through November 2018. All of the data comes from the Office for Registration of Medicinal Products, Medical Devices and Biocidal Products, 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 Poland.
  • Notas adicionales en la data
  • Acción
    Ningbo Greetmed Medica safety notice regarding the withdrawal from the market and the use of umbilical iron clamps, series No. 20161026
Notificaciones De Seguridad De Campo acerca de elisio h dialyzers.
  • Tipo de evento
    Field Safety Notice
  • ID del evento
    2157
  • Fecha
    2011-01-25
  • País del evento
    Poland
  • Fuente del evento
    ORMPMDBP
  • URL de la fuente del evento
    http://www.urpl.gov.pl/pl/notatka-bezpiecze%C5%84stwa-firmy-nipro-dotycz%C4%85ca-dializator%C3%B3w-elisio-h
  • Notas / Alertas
    Polish data is current through November 2018. All of the data comes from the Office for Registration of Medicinal Products, Medical Devices and Biocidal Products, 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 Poland.
  • Notas adicionales en la data
  • Acción
    NIPRO safety note regarding ELISIO H. dialyzers
Notificaciones De Seguridad De Campo acerca de mustang walking help
  • Tipo de evento
    Field Safety Notice
  • ID del evento
    2486
  • Fecha
    2012-07-20
  • País del evento
    Poland
  • Fuente del evento
    ORMPMDBP
  • URL de la fuente del evento
    http://www.urpl.gov.pl/pl/notatka-bezpiecze%C5%84stwa-firmy-r82-dotycz%C4%85ca-pomocy-do-chodzenia-mustang
  • Notas / Alertas
    Polish data is current through November 2018. All of the data comes from the Office for Registration of Medicinal Products, Medical Devices and Biocidal Products, 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 Poland.
  • Notas adicionales en la data
  • Acción
    R82 A / S safety note on Mustang walking aid
Notificaciones De Seguridad De Campo acerca de nps25 and nps50 cytology platforms with version 4 ...
  • Tipo de evento
    Field Safety Notice
  • ID del evento
    935
  • Fecha
    2017-03-17
  • País del evento
    Poland
  • Fuente del evento
    ORMPMDBP
  • URL de la fuente del evento
    http://www.urpl.gov.pl/pl/notatka-bezpiecze%C5%84stwa-firmy-novacyt-sa-dotycz%C4%85ca-platformy-do-cytologii-nps25-i-nps50-z
  • Notas / Alertas
    Polish data is current through November 2018. All of the data comes from the Office for Registration of Medicinal Products, Medical Devices and Biocidal Products, 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 Poland.
  • Notas adicionales en la data
  • Acción
    Novacyt SA safety note regarding the NPS25 and NPS50 cytology platform with version 4 software
Notificaciones De Seguridad De Campo acerca de trocar cannula without 23g valve and infusion cann...
  • Tipo de evento
    Field Safety Notice
  • ID del evento
    2336
  • Fecha
    2012-05-31
  • País del evento
    Poland
  • Fuente del evento
    ORMPMDBP
  • URL de la fuente del evento
    http://www.urpl.gov.pl/pl/notatka-bezpiecze%C5%84stwa-firmy-alcon-laboratories-inc-dotycz%C4%85ca-kaniuli-trokara-bez-zaworu-23g-i-0
  • Notas / Alertas
    Polish data is current through November 2018. All of the data comes from the Office for Registration of Medicinal Products, Medical Devices and Biocidal Products, 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 Poland.
  • Notas adicionales en la data
  • Acción
    Safety note from Alcon Laboratories Inc. on the trocar cannula without the 23G valve and the infusion cannula included in the Alcon Custom Pak packages
Notificaciones De Seguridad De Campo acerca de trocar cannula without 23g valve and infusion cann...
  • Tipo de evento
    Field Safety Notice
  • ID del evento
    1968
  • Fecha
    2012-05-31
  • País del evento
    Poland
  • Fuente del evento
    ORMPMDBP
  • URL de la fuente del evento
    http://www.urpl.gov.pl/pl/notatka-bezpiecze%C5%84stwa-firmy-alcon-laboratories-inc-dotycz%C4%85ca-kaniuli-trokara-bez-zaworu-23g-i
  • Notas / Alertas
    Polish data is current through November 2018. All of the data comes from the Office for Registration of Medicinal Products, Medical Devices and Biocidal Products, 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 Poland.
  • Notas adicionales en la data
  • Acción
    Safety note from Alcon Laboratories Inc. concerning the trocar cannula without the 23G valve and the infusion cannula included in the packages (Accurus and Constellation) 23G TotalPlus Pak and 23G Combined Procedure Pack (0.9 mm and 1.1 mm)
Notificaciones De Seguridad De Campo acerca de acrysof cachet phakic lenses
  • Tipo de evento
    Field Safety Notice
  • ID del evento
    1717
  • Fecha
    2012-02-09
  • País del evento
    Poland
  • Fuente del evento
    ORMPMDBP
  • URL de la fuente del evento
    http://www.urpl.gov.pl/pl/notatka-bezpiecze%C5%84stwa-firmy-alcon-dotycz%C4%85ca-soczewek-acrysof-cachet-phakic
  • Notas / Alertas
    Polish data is current through November 2018. All of the data comes from the Office for Registration of Medicinal Products, Medical Devices and Biocidal Products, 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 Poland.
  • Notas adicionales en la data
  • Acción
    Alcon safety note regarding AcrySof CACHET Phakic lenses
Notificaciones De Seguridad De Campo acerca de acrysof cachet phakic lenses
  • Tipo de evento
    Field Safety Notice
  • ID del evento
    2042
  • Fecha
    2012-07-10
  • País del evento
    Poland
  • Fuente del evento
    ORMPMDBP
  • URL de la fuente del evento
    http://www.urpl.gov.pl/pl/notatka-bezpiecze%C5%84stwa-firmy-alcon-dotycz%C4%85ca-soczewek-acrysof-cachet-phakic-uaktualnienie-notatki-z
  • Notas / Alertas
    Polish data is current through November 2018. All of the data comes from the Office for Registration of Medicinal Products, Medical Devices and Biocidal Products, 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 Poland.
  • Notas adicionales en la data
  • Acción
    Alcon safety note regarding Acrysof CACHET Phakic lenses - update of the memo from 9/02/2012
Notificaciones De Seguridad De Campo acerca de alcon acrysof cachet phakic lenses
  • Tipo de evento
    Field Safety Notice
  • ID del evento
    1729
  • Fecha
    2013-11-08
  • País del evento
    Poland
  • Fuente del evento
    ORMPMDBP
  • URL de la fuente del evento
    http://www.urpl.gov.pl/pl/notatka-bezpiecze%C5%84stwa-firmy-alcon-dotycz%C4%85ca-soczewek-alcon-acrysof-cachet-phakic
  • Notas / Alertas
    Polish data is current through November 2018. All of the data comes from the Office for Registration of Medicinal Products, Medical Devices and Biocidal Products, 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 Poland.
  • Notas adicionales en la data
  • Acción
    Alcon safety note regarding Alcon AcrySof CACHET Phakic lenses
Notificaciones De Seguridad De Campo acerca de alcon acrysof cachet phakic lenses
  • Tipo de evento
    Field Safety Notice
  • ID del evento
    1260
  • Fecha
    2013-04-16
  • País del evento
    Poland
  • Fuente del evento
    ORMPMDBP
  • URL de la fuente del evento
    http://www.urpl.gov.pl/pl/notatka-bezpiecze%C5%84stwa-firmy-alcon-laboratories-dotycz%C4%85ca-soczewek-alcon-acrysof-cachet-phakic
  • Notas / Alertas
    Polish data is current through November 2018. All of the data comes from the Office for Registration of Medicinal Products, Medical Devices and Biocidal Products, 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 Poland.
  • Notas adicionales en la data
  • Acción
    Alcon Laboratories safety note regarding Alcon AcrySof CACHET Phakic lenses
Notificaciones De Seguridad De Campo acerca de alcon or endure luxor e71 ophthalmic microscopes a...
  • Tipo de evento
    Field Safety Notice
  • ID del evento
    397
  • Fecha
    2018-08-09
  • País del evento
    Poland
  • Fuente del evento
    ORMPMDBP
  • URL de la fuente del evento
    http://www.urpl.gov.pl/pl/notatka-bezpiecze%C5%84stwa-2018014-itc-firmy-alcon-laboratories-dotycz%C4%85ca-mikroskop%C3%B3w-okulistycznych
  • Notas / Alertas
    Polish data is current through November 2018. All of the data comes from the Office for Registration of Medicinal Products, Medical Devices and Biocidal Products, 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 Poland.
  • Notas adicionales en la data
  • Acción
    Safety note (2018.014-ITC) from Alcon Laboratories for Alcon or Endure LuxOR E71 ophthalmic microscopes and Alcon or Endure LuxOR E71 Q-Vue ophthalmic microscopes
Notificaciones De Seguridad De Campo acerca de constellation vision system
  • Tipo de evento
    Field Safety Notice
  • ID del evento
    1924
  • Fecha
    2010-05-20
  • País del evento
    Poland
  • Fuente del evento
    ORMPMDBP
  • URL de la fuente del evento
    http://www.urpl.gov.pl/pl/komunikat-firmy-alcon-dotycz%C4%85cy-systemu-constellation-vision-20052010
  • Notas / Alertas
    Polish data is current through November 2018. All of the data comes from the Office for Registration of Medicinal Products, Medical Devices and Biocidal Products, 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 Poland.
  • Notas adicionales en la data
  • Acción
    Alcon's announcement regarding the Constellation Vision system (20/05/2010)
Notificaciones De Seguridad De Campo acerca de ciba vision corporation on softperm contact lenses
  • Tipo de evento
    Field Safety Notice
  • ID del evento
    2030
  • Fecha
    2010-06-11
  • País del evento
    Poland
  • Fuente del evento
    ORMPMDBP
  • URL de la fuente del evento
    http://www.urpl.gov.pl/pl/komunikat-firmy-ciba-vision-corporation-dotycz%C4%85cy-soczewek-kontaktowych-softperm-11062010
  • Notas / Alertas
    Polish data is current through November 2018. All of the data comes from the Office for Registration of Medicinal Products, Medical Devices and Biocidal Products, 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 Poland.
  • Notas adicionales en la data
  • Acción
    Message from CIBA VISION Corporation regarding Softperm contact lenses (11/06/2010)
Notificaciones De Seguridad De Campo acerca de fake fresh look colorblends contact lenses
  • Tipo de evento
    Field Safety Notice
  • ID del evento
    2024
  • Fecha
    2013-04-08
  • País del evento
    Poland
  • Fuente del evento
    ORMPMDBP
  • URL de la fuente del evento
    http://www.urpl.gov.pl/pl/komunikat-w-sprawie-sfa%C5%82szowanych-soczewek-kontaktowych-fresh-look-colorblends
  • Notas / Alertas
    Polish data is current through November 2018. All of the data comes from the Office for Registration of Medicinal Products, Medical Devices and Biocidal Products, 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 Poland.
  • Notas adicionales en la data
  • Acción
    Communication regarding fake Fresh Look Colorblends contact lenses
Notificaciones De Seguridad De Campo acerca de discontinuation of alcon acrysof cachet phakic lenses
  • Tipo de evento
    Field Safety Notice
  • ID del evento
    2676
  • Fecha
    2014-10-21
  • País del evento
    Poland
  • Fuente del evento
    ORMPMDBP
  • URL de la fuente del evento
    http://www.urpl.gov.pl/pl/notatka-bezpiecze%C5%84stwa-firmy-alcon-dotycz%C4%85ca-zaprzestania-wytwarzania-soczewek-alcon-acrysof-cachet
  • Notas / Alertas
    Polish data is current through November 2018. All of the data comes from the Office for Registration of Medicinal Products, Medical Devices and Biocidal Products, 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 Poland.
  • Notas adicionales en la data
  • Acción
    Alcon safety note regarding the discontinuation of Alcon AcrySof CACHET Phakic lenses
Notificaciones De Seguridad De Campo acerca de lx3 floor microscope stand used with the luxor oph...
  • Tipo de evento
    Field Safety Notice
  • ID del evento
    612
  • Fecha
    2017-06-14
  • País del evento
    Poland
  • Fuente del evento
    ORMPMDBP
  • URL de la fuente del evento
    http://www.urpl.gov.pl/pl/notatka-bezpiecze%C5%84stwa-firmy-alcon-laboratories-inc-dotycz%C4%85ca-statyw-pod%C5%82ogowego-mikroskopu-lx3
  • Notas / Alertas
    Polish data is current through November 2018. All of the data comes from the Office for Registration of Medicinal Products, Medical Devices and Biocidal Products, 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 Poland.
  • Notas adicionales en la data
  • Acción
    Safety note from Alcon Laboratories Inc. regarding the LX3 floor stand microscope used with the LuxOR ophthalmic microscope
Notificaciones De Seguridad De Campo acerca de lx3 microscope floor stand
  • Tipo de evento
    Field Safety Notice
  • ID del evento
    2445
  • Fecha
    2015-08-21
  • País del evento
    Poland
  • Fuente del evento
    ORMPMDBP
  • URL de la fuente del evento
    http://www.urpl.gov.pl/pl/notatka-bezpiecze%C5%84stwa-firmy-alcon-laboratories-inc-dotycz%C4%85ca-statywu-pod%C5%82ogowego-mikroskopu-lx3
  • Notas / Alertas
    Polish data is current through November 2018. All of the data comes from the Office for Registration of Medicinal Products, Medical Devices and Biocidal Products, 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 Poland.
  • Notas adicionales en la data
  • Acción
    Safety note from Alcon Laboratories Inc. regarding the LX3 microscope floor stand
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