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  • Dispositivo 8
  • Fabricante 2
  • Evento 124969
  • Implante 0
Notificaciones De Seguridad De Campo acerca de devon treatment lamp covers
  • Tipo de evento
    Field Safety Notice
  • ID del evento
    953
  • Fecha
    2016-10-28
  • 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-medtronic-dotycz%C4%85ca-aktualizacji-instrukcji-u%C5%BCywania-os%C5%82on-uchwyt%C3%B3w
  • 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
    Medtronic safety note regarding the update of instructions for use of Devon treatment lamp covers
Notificaciones De Seguridad De Campo acerca de activa pc, activa pc + s, activa rc, activa sc, al...
  • Tipo de evento
    Field Safety Notice
  • ID del evento
    1796
  • Fecha
    2014-02-25
  • 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-medtronic-dotycz%C4%85ca-aktualizacji-oznakowania-urz%C4%85dze%C5%84-do
  • 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
    Medtronic safety note regarding the update of the labeling of devices for neurostimulation Activa PC, Activa PC + S, Activa RC, Activa SC, all Restore devices (including SureScan), PrimeADVANCED, PrimeADVANCED SureScan MRI and Itrel 4
Notificaciones De Seguridad De Campo acerca de tissue stapler. trs duo.
  • Tipo de evento
    Field Safety Notice
  • ID del evento
    2078
  • Fecha
    2012-01-25
  • 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-covidien-dotycz%C4%85ca-stosowania-%C5%82adunk%C3%B3w-do-staplera-tkankowego-duet-trs
  • 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
    Covidien's safety note regarding the use of cargo for the TRS tissue stapler.
Notificaciones De Seguridad De Campo acerca de implantable synchromed® infusion pump
  • Tipo de evento
    Field Safety Notice
  • ID del evento
    1347
  • Fecha
    2012-11-15
  • 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-medtronic-dotycz%C4%85ca-stosowanie-niezatwierdzonych-lek%C3%B3w-w-po%C5%82%C4%85czeniu-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
    Medtronic safety note regarding the use of unapproved medication in combination with an implantable SynchroMed® infusion pump
Notificaciones De Seguridad De Campo acerca de enveo r guide catheter system, enveor-l and enveor...
  • Tipo de evento
    Field Safety Notice
  • ID del evento
    421
  • Fecha
    2016-08-16
  • 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-medtronic-dotycz%C4%85ca-stosowania-systemu-cewnika-prowadz%C4%85cego-medtronic-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
    Medtronic safety note on the use of the Medtronic EnVeo R guide catheter system, ENVEOR-L and ENVEOR-LC models
Notificaciones De Seguridad De Campo acerca de pipeline embolization device
  • Tipo de evento
    Field Safety Notice
  • ID del evento
    1314
  • Fecha
    2012-12-28
  • 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-covidien-dotycz%C4%85ca-stosowania-urz%C4%85dzenia-do-embolizacji-pipeline
  • 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
    Covidien safety note regarding the use of the Pipeline embolization device
Notificaciones De Seguridad De Campo acerca de vitatron
  • Tipo de evento
    Field Safety Notice
  • ID del evento
    1245
  • Fecha
    2007-03-08
  • País del evento
    Poland
  • Fuente del evento
    ORMPMDBP
  • URL de la fuente del evento
    http://www.urpl.gov.pl/pl/informacja-o-stymulatorach-firmy-vitatron-08032007
  • 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
    Information on VITATRON stimulators (08.03.2007)
Notificaciones De Seguridad De Campo acerca de clearify laparoscope cleaning system
  • Tipo de evento
    Field Safety Notice
  • ID del evento
    62
  • Fecha
    2016-10-28
  • 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-medtronic-dotycz%C4%85ca-wycofania-z-obrotu-i-u%C5%BCywania-niekt%C3%B3rych-partii-1
  • 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
    Medtronic safety note regarding the withdrawal and use of some lots of the Clearify laparoscopic cleaning system (code no. 21-345)
Notificaciones De Seguridad De Campo acerca de heartware hvad system drivers with serial numbers ...
  • Tipo de evento
    Field Safety Notice
  • ID del evento
    56
  • Fecha
    2018-02-28
  • País del evento
    Poland
  • Fuente del evento
    ORMPMDBP
  • URL de la fuente del evento
    http://www.urpl.gov.pl/pl/notatka-bezpiecze%C5%84stwa-fsca-jan2017-firmy-heartware-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
    Safety note (FSCA JAN2017) from HeartWare regarding the withdrawal and use of the HeartWare HVAD system drivers with serial numbers lower than CON300000
Notificaciones De Seguridad De Campo acerca de angioplastic energy chains cougar, zinger, thunder...
  • Tipo de evento
    Field Safety Notice
  • ID del evento
    1283
  • Fecha
    2013-10-24
  • 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-medtronic-dotycz%C4%85ca-wycofania-z-obrotu-i-z-u%C5%BCywania-prowadnik%C3%B3w
  • 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
    Medtronic safety note regarding withdrawal and use of the COUGAR, ZINGER, THUNDER and ProVia angioplasty tubes and ATTAIN HYBRID
Notificaciones De Seguridad De Campo acerca de vectris screen electrode kits and vectris surescan...
  • Tipo de evento
    Field Safety Notice
  • ID del evento
    201
  • Fecha
    2018-08-20
  • País del evento
    Poland
  • Fuente del evento
    ORMPMDBP
  • URL de la fuente del evento
    http://www.urpl.gov.pl/pl/notatka-bezpiecze%C5%84stwa-fa822-firmy-medtronic-dotycz%C4%85ca-wycofania-z-obrotu-i-z-u%C5%BCywania-niekt%C3%B3rych
  • 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
    Medtronic safety note (FA822) concerning the withdrawal and use of certain series of Vectris screen electrode kits and Vectris SureScan electrode kits
Notificaciones De Seguridad De Campo acerca de controllable flexcath select, model 990065, series...
  • Tipo de evento
    Field Safety Notice
  • ID del evento
    1162
  • Fecha
    2015-03-06
  • 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-medtronic-dotycz%C4%85ca-wycofania-z-obrotu-i-u%C5%BCywania-sterowalnych-koszulek
  • 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
    Medtronic safety note regarding withdrawal and use of FlexCath Select tilted T-shirts, model 990065, 54790, 54860, 54876, 54877, 54878, 72417 and 72419
Notificaciones De Seguridad De Campo acerca de covidien endo gia ultra universal staple holders w...
  • Tipo de evento
    Field Safety Notice
  • ID del evento
    1697
  • Fecha
    2015-12-18
  • 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-covidien-dotycz%C4%85ca-wycofania-z-obrotu-i-u%C5%BCywania-uchwyt%C3%B3w-stapler%C3%B3w
  • 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
    Covidien safety notice regarding the withdrawal and use of Covidien Endo GIA Ultra Universal staple holders with specific catalog numbers and lot numbers
Notificaciones De Seguridad De Campo acerca de deep brain stimulation electrode sets
  • Tipo de evento
    Field Safety Notice
  • ID del evento
    2755
  • Fecha
    2013-06-25
  • 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-medtronic-dotycz%C4%85ca-wycofania-z-obrotu-i-z-u%C5%BCywania-zestaw%C3%B3w-elektrod
  • 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
    Medtronic safety note regarding withdrawal and use of deep brain stimulation electrode sets (DBS)
Notificaciones De Seguridad De Campo acerca de deep brain stimulation electrode sets , models 338...
  • Tipo de evento
    Field Safety Notice
  • ID del evento
    982
  • Fecha
    2017-09-19
  • 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-medtronic-dotycz%C4%85ca-wycofania-z-obrotu-i-u%C5%BCywania-zestaw%C3%B3w-elektrod-do
  • 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
    Medtronic safety note regarding withdrawal and use of deep brain stimulation electrode kits (DBS), models 3387, 3389 and 3391
Notificaciones De Seguridad De Campo acerca de dgp-hp rfa disposable earthing plates and cool-tip...
  • Tipo de evento
    Field Safety Notice
  • ID del evento
    1118
  • Fecha
    2012-09-24
  • 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-covidien-dotycz%C4%85ca-wycofania-z-obrotu-i-z-u%C5%BCywania-jednorazowych-p%C5%82ytek
  • 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
    Covidien safety notice regarding withdrawal and use of DGP-HP RFA disposable earthing plates and Cool-tip RFA electrode sets
Notificaciones De Seguridad De Campo acerca de in.pact amphirion balloon catheters
  • Tipo de evento
    Field Safety Notice
  • ID del evento
    1263
  • Fecha
    2013-11-21
  • 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-medtronic-dotycz%C4%85ca-wycofania-z-obrotu-i-z-u%C5%BCywania-cewnik%C3%B3w-balonowych
  • 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
    Medtronic safety note regarding withdrawal and use of IN.PACT Amphirion balloon catheters
Notificaciones De Seguridad De Campo acerca de oscar atar reusable extension cables for an extern...
  • Tipo de evento
    Field Safety Notice
  • ID del evento
    878
  • Fecha
    2017-08-30
  • 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-medtronic-dotycz%C4%85ca-wycofania-z-obrotu-i-z-u%C5%BCywania-kabli
  • 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
    Medtronic safety note regarding the withdrawal and use of Oscar ATAR reusable extension cables for an external pulse generator (EPG), models 53912, 53912A and 53912D
Notificaciones De Seguridad De Campo acerca de polysorb braided absorbable sutures, endo stitch i...
  • Tipo de evento
    Field Safety Notice
  • ID del evento
    850
  • Fecha
    2017-05-26
  • 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-medtronic-dotycz%C4%85ca-wycofania-z-obrotu-i-z-u%C5%BCywania-niekt%C3%B3rych-serii-2
  • 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
    Medtronic safety note regarding the withdrawal and use of certain batches: Polysorb braided absorbable sutures, Polysorb Endo Stitch insertion modules, Maxon and Biosyn monofilament absorbable sutures
Notificaciones De Seguridad De Campo acerca de amphirion deep balloon catheter
  • Tipo de evento
    Field Safety Notice
  • ID del evento
    1656
  • Fecha
    2015-11-05
  • 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-medtronic-dotycz%C4%85ca-wycofania-z-obrotu-i-z-u%C5%BCywania-okre%C5%9Blonych-partii
  • 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
    Medtronic safety notice regarding withdrawal and use of specific batches of the Amphirion Deep balloon catheter
Notificaciones De Seguridad De Campo acerca de symplicity model rdn006 catheters
  • Tipo de evento
    Field Safety Notice
  • ID del evento
    2681
  • Fecha
    2012-08-20
  • 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-medtronic-inc-dotycz%C4%85ca-wycofania-z-obrotu-i-z-u%C5%BCywania-cewnik%C3%B3w
  • 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
    Security note from Medtronic Inc. concerning the withdrawal and use of the Symplicity Model RDN006 catheters
Notificaciones De Seguridad De Campo acerca de synchromed ii infusion pumps
  • Tipo de evento
    Field Safety Notice
  • ID del evento
    607
  • Fecha
    2018-01-05
  • País del evento
    Poland
  • Fuente del evento
    ORMPMDBP
  • URL de la fuente del evento
    http://www.urpl.gov.pl/pl/notatka-bezpiecze%C5%84stwa-fa794-firmy-medtronic-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
    Medtronic safety note (FA794) regarding withdrawal from the market and use of uninoculated infusion pumps SynchroMed II
Notificaciones De Seguridad De Campo acerca de mmt-326a and mmt-332a insulin reservoirs for parad...
  • Tipo de evento
    Field Safety Notice
  • ID del evento
    2674
  • Fecha
    2013-07-17
  • 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-medtronic-minimed-dotycz%C4%85ca-wycofania-z-obrotu-i-z-u%C5%BCywania-zbiornik%C3%B3w
  • 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
    Medtronic MiniMed safety note regarding the withdrawal and use of MMT-326A and MMT-332A insulin reservoirs for Paradigm insulin pumps
Notificaciones De Seguridad De Campo acerca de 11088329 series of bone access needles kyphon size 11
  • Tipo de evento
    Field Safety Notice
  • ID del evento
    1967
  • Fecha
    2015-07-09
  • 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-medtronic-dotycz%C4%85ca-wycofania-z-obrotu-i-u%C5%BCywania-serii-11088329-igie%C5%82
  • 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
    Medtronic safety note regarding the withdrawal and use of the 11088329 series bone access needles KYPHON size 11 (model A02A) from Argon Medical
Notificaciones De Seguridad De Campo acerca de bio-cal temperature controller, models 370 and 370i
  • Tipo de evento
    Field Safety Notice
  • ID del evento
    548
  • Fecha
    2018-02-22
  • País del evento
    Poland
  • Fuente del evento
    ORMPMDBP
  • URL de la fuente del evento
    http://www.urpl.gov.pl/pl/notatka-bezpiecze%C5%84stwa-fa801-firmy-medtronic-dotycz%C4%85ca-wycofania-z-obrotu-i-z-u%C5%BCywania-wszystkich
  • 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
    Medtronic safety note (FA801) regarding the withdrawal and use of all serial numbers of the Bio-Cal temperature controller, models 370 and 370I
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Aviso

Los dispositivos médicos ayudan con el diagnóstico, la prevención y el tratamiento de muchas lesiones y enfermedades. A través de la International Medical Devices Database no estamos sugiriendo que compañías u otras entidades mencionadas en la base de datos hayan sido parte de una conducta ilegal o hayan actuado de manera impropia. Un mismo dispositivo médico puede tener distintos nombres en diferentes países. Esta base de datos no busca proporcionar asesoría médica. Los pacientes deben consultar con sus médicos para determinar si la data contiene información relevante y si la misma tiene implicaciones médicas para ellos.

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