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  • Dispositivo 2677
  • Fabricante 2677
  • Evento 2803
  • Implante 0
Notificaciones De Seguridad De Campo acerca de drains for redon wounds
  • Tipo de evento
    Field Safety Notice
  • ID del evento
    1220
  • Fecha
    2008-05-07
  • País del evento
    Poland
  • Fuente del evento
    ORMPMDBP
  • URL de la fuente del evento
    http://www.urpl.gov.pl/pl/komunikat-firmy-wsm-galmed-dotycz%C4%85cy-dren%C3%B3w-do-ran-typu-redon-07052008
  • 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
    Announcement of the WSM GALMED company regarding drains for REDON wounds (07.05.2008)
Notificaciones De Seguridad De Campo acerca de nebu muco 7% naci inhalation solution, series 10816
  • Tipo de evento
    Field Safety Notice
  • ID del evento
    438
  • Fecha
    2018-02-05
  • 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-zak%C5%82ady-farmaceutyczne-polpharma-sa-dotycz%C4%85ca-wycofania-z-obrotu-wyrobu
  • 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
    Memorandum of safety of the Polpharma Pharmaceutical Plant concerning the withdrawal from the market of the medical device Nebu Muco 7% NaCI inhalation solution, series 10816
Notificaciones De Seguridad De Campo acerca de argenton optic eyelid spray with the a02 series
  • Tipo de evento
    Field Safety Notice
  • ID del evento
    238
  • Fecha
    2016-12-07
  • 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-solinea-sp-z-o-o-sp-k-dotycz%C4%85ca-wycofania-z-obrotu-sprayu-na-powieki
  • 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 Solinea Sp. z oo Sp. k. concerning the withdrawal of the Argenton optic eyelid spray with the A02 series
Notificaciones De Seguridad De Campo acerca de tracheostomy tubes without a cuff, no. category be...
  • Tipo de evento
    Field Safety Notice
  • ID del evento
    1207
  • Fecha
    2014-07-24
  • 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-sumi-zak%C5%82ad-tworzyw-sztucznych-k-rek-krzanowski-sj-dotycz%C4%85ca-wycofania
  • 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 of the SUMI company Zakład Tworzyw Sztucznych K. Rek A. Krzanowski SJ concerning withdrawal from the market and use of tracheostomy tubes without a cuff, no. category beginning with figures 33 and from 10.01.01 to 06.16.06
Notificaciones De Seguridad De Campo acerca de glosal throat spray series 2013-03-05
  • Tipo de evento
    Field Safety Notice
  • ID del evento
    1403
  • Fecha
    2014-10-31
  • 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-arkona-trade-and-science-grzegorz-kalbarczyk-sp-j-dotycz%C4%85ca-wycofania-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
    Security memo of ARKONA Trade and Science Grzegorz Kalbarczyk Sp. J. concerning the withdrawal from the market and use of the GLOSAL throat spray series 2013-03-05
Notificaciones De Seguridad De Campo acerca de ectodose x721b inhalation solution
  • Tipo de evento
    Field Safety Notice
  • ID del evento
    683
  • Fecha
    2018-07-19
  • 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-solinea-sp-z-oo-sp-k-dotycz%C4%85ca-wycofania-z-obrotu-i-u%C5%BCywania-roztworu
  • 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 Solinea Sp. z oo Sp. K. regarding the withdrawal from use and use of the Ectodose X721B inhalation solution manufactured by the Bitop AG company
Notificaciones De Seguridad De Campo acerca de nasal spray solik complex
  • Tipo de evento
    Field Safety Notice
  • ID del evento
    1665
  • Fecha
    2014-10-31
  • 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-arkona-trade-and-science-grzegorz-kalbarczyk-sp-j-dotycz%C4%85ca-wycofania-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
    Security memo of ARKONA Trade and Science Grzegorz Kalbarczyk Sp. J. concerning the withdrawal from use and use of some series of nasal spray SOLIK complex
Notificaciones De Seguridad De Campo acerca de nabatoff varicose veins
  • Tipo de evento
    Field Safety Notice
  • ID del evento
    742
  • Fecha
    2017-06-20
  • 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-chirstom-dotycz%C4%85ca-wycofania-z-obrotu-i-z-u%C5%BCywania-niekt%C3%B3rych-serii
  • 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
    Chirstom safety note regarding the withdrawal and use of certain series of Nabatoff varicose veins
Notificaciones De Seguridad De Campo acerca de sengstaken probes and urological guides of the lun...
  • Tipo de evento
    Field Safety Notice
  • ID del evento
    1111
  • Fecha
    2013-11-28
  • 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-skamex-sp-z-oo-ska-dotycz%C4%85ca-wycofania-z-obrotu-i-z-u%C5%BCywania-sond
  • 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 Skamex Sp. z o. o. SKA regarding the withdrawal and use of Sengstaken probes and urological guides, the TeleflexMedical Lunderquist
Notificaciones De Seguridad De Campo acerca de reusable sureflex fibers and accessories for fiber...
  • Tipo de evento
    Field Safety Notice
  • ID del evento
    1874
  • Fecha
    2015-07-21
  • 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-american-medical-systems-dotycz%C4%85ca-wycofania-z-obrotu-i-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
    American Medical Systems safety notice regarding the withdrawal and use of reusable SureFlex fibers and fiber restoration accessories
Notificaciones De Seguridad De Campo acerca de reinforced intubation tubes, with the serial numbe...
  • Tipo de evento
    Field Safety Notice
  • ID del evento
    801
  • Fecha
    2017-02-03
  • 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-sumi-dotycz%C4%85ca-wycofania-z-obrotu-i-z-u%C5%BCywania-rurek-intubacyjnych-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
    SUMI's safety note regarding the withdrawal from the market and the use of reinforced intubation tubes, with the batch number from 12/01/01 to 16/12/12, in sizes 2,0 / 2,5 / 3,0
Notificaciones De Seguridad De Campo acerca de orthopedic products
  • Tipo de evento
    Field Safety Notice
  • ID del evento
    961
  • Fecha
    2016-06-17
  • 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-arno-med-sp-z-oo-dotycz%C4%85ca-wycofania-z-obrotu-i-u%C5%BCywania-wyrob%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 of the company ARNO-MED Sp. z oo regarding the withdrawal from the market and use of orthopedic products by NARANG MEDICAL LIMITED, New Delhi, India
Notificaciones De Seguridad De Campo acerca de lot no. 20141220 of idle band gauze 1 mx 1 m, cata...
  • Tipo de evento
    Field Safety Notice
  • ID del evento
    1191
  • Fecha
    2015-06-23
  • 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-polmil-sp%C3%B3%C5%82ka-z-oo-dotycz%C4%85ca-wycofania-z-obrotu-i-u%C5%BCywania-serii-nr
  • 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
    Polmil Spółka z oo security notice concerning the withdrawal from circulation and use of lot No. 20141220 of Inertium gauze 1 mx 1 m, catalog number PSM5034s, Xiantao
Notificaciones De Seguridad De Campo acerca de disposable injection needles lot 2015-01
  • Tipo de evento
    Field Safety Notice
  • ID del evento
    754
  • Fecha
    2017-11-13
  • 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-unidem-ltd-sk-dotycz%C4%85ca-wycofania-z-obrotu-i-z-u%C5%BCywania-igie%C5%82-0
  • 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
    Security note from Unidem Ltd SK concerning withdrawal from the market and use of disposable injection needles LOT 2015-01
Notificaciones De Seguridad De Campo acerca de disposable injection needles lot 2015-01
  • Tipo de evento
    Field Safety Notice
  • ID del evento
    515
  • Fecha
    2017-11-10
  • 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-unidem-ltd-sk-dotycz%C4%85ca-wycofania-z-obrotu-i-z-u%C5%BCywania-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
    Security note from Unidem Ltd SK concerning withdrawal from the market and use of disposable injection needles LOT 2015-01
Notificaciones De Seguridad De Campo acerca de hyacorp l, hyacorp h 1000, hyacorp hs 500
  • Tipo de evento
    Field Safety Notice
  • ID del evento
    1204
  • Fecha
    2013-08-29
  • 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-biosciense-gmbh-dotycz%C4%85ca-wycofania-z-obrotu-i-z-u%C5%BCywania-hyacorp-l
  • 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
    Biosciense GmbH safety notice regarding the withdrawal and use of HYAcorp L, HYAcorp H 1000, HYAcorp HS 500
Notificaciones De Seguridad De Campo acerca de vego fine injection needles
  • Tipo de evento
    Field Safety Notice
  • ID del evento
    1794
  • Fecha
    2007-08-06
  • País del evento
    Poland
  • Fuente del evento
    ORMPMDBP
  • URL de la fuente del evento
    http://www.urpl.gov.pl/pl/powiadomienie-w-sprawie-igie%C5%82-iniekcyjnych-vego-fine-06082007
  • 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
    Notification on Vego Fine injection needles (06.08.2007)
Notificaciones De Seguridad De Campo acerca de vego fine injection needles
  • Tipo de evento
    Field Safety Notice
  • ID del evento
    2668
  • Fecha
    2007-08-10
  • País del evento
    Poland
  • Fuente del evento
    ORMPMDBP
  • URL de la fuente del evento
    http://www.urpl.gov.pl/pl/komunikat-w-sprawie-igie%C5%82-iniekcyjnych-vego-fine-10082007
  • 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 on Vego Fine injection needles (10/08/2007)
Notificaciones De Seguridad De Campo acerca de opokan med warming patch
  • Tipo de evento
    Field Safety Notice
  • ID del evento
    1210
  • Fecha
    2015-02-16
  • 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-j-chodacki-misztal-%E2%80%9Emedica%E2%80%9D-sp%C3%B3%C5%82ka-jawna-dotycz%C4%85ca-stosowania-plastra
  • 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
    Memo of the company J. CHODACKI, A. MISZTAL "MEDICA" General partnership regarding the use of the heating patch Opokan MED
Notificaciones De Seguridad De Campo acerca de electrosurgical devices for arthroscopy with some ...
  • Tipo de evento
    Field Safety Notice
  • ID del evento
    1068
  • Fecha
    2018-07-03
  • País del evento
    Poland
  • Fuente del evento
    ORMPMDBP
  • URL de la fuente del evento
    http://www.urpl.gov.pl/pl/notatka-bezpiecze%C5%84stwa-1fsca2018-firmy-emed-sp-z-oo-sp-k-dotycz%C4%85ca-aktualizacji-oprogramowania-rf
  • 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
    Notatka bezpieczeństwa (1 / FSCA / 2018) of the company EMED Sp. z oo Sp. K. on updating the RF software of electrosurgical apparatus for arthroscopy with some serial numbers
Notificaciones De Seguridad De Campo acerca de umbilical cord clamps
  • Tipo de evento
    Field Safety Notice
  • ID del evento
    2256
  • Fecha
    2008-03-12
  • País del evento
    Poland
  • Fuente del evento
    ORMPMDBP
  • URL de la fuente del evento
    http://www.urpl.gov.pl/pl/komunikat-firmy-sonda-sp-j-dotycz%C4%85cy-zaciskaczy-do-p%C4%99powiny-produkcji-firmy-yangzhou-wuyang-medical
  • 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
    The announcement of the company SONDA Sp. j. on umbilical cuffs manufactured by Yangzhou Wuyang Medical Equipment Co., Ltd., China. (12.03.2008)
Notificaciones De Seguridad De Campo acerca de umbilical cord clamps
  • Tipo de evento
    Field Safety Notice
  • ID del evento
    2687
  • Fecha
    2008-03-12
  • País del evento
    Poland
  • Fuente del evento
    ORMPMDBP
  • URL de la fuente del evento
    http://www.urpl.gov.pl/pl/komunikat-firmy-irhen-sp-z-oo-dotycz%C4%85cy-zaciskaczy-do-p%C4%99powiny-produkcji-firmy-changzhou-yishou
  • 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
    Announcement of the company Irhen Sp. z o. o. concerning umbilical cord clamps made by Changzhou Yishou Medical Apparatus Co., Ltd., China. (12.03.2008)
Notificaciones De Seguridad De Campo acerca de two-way chemotherapy device, lot no. 15 01 130
  • Tipo de evento
    Field Safety Notice
  • ID del evento
    2727
  • Fecha
    2015-08-07
  • 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-lzf-polfa-dotycz%C4%85ca-wycofania-z-obrotu-i-z-u%C5%BCywania-przyrz%C4%85du-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
    LZF Polfa's safety note regarding the withdrawal from the market and use of a two-way chemotherapy device, lot no. 15 01 130
Notificaciones De Seguridad De Campo acerca de tracheostomy tubes
  • Tipo de evento
    Field Safety Notice
  • ID del evento
    2243
  • Fecha
    2009-09-10
  • País del evento
    Poland
  • Fuente del evento
    ORMPMDBP
  • URL de la fuente del evento
    http://www.urpl.gov.pl/pl/komunikat-firmy-pyramed-sp-z-oo-o-wstrzymaniu-obrotu-i-u%C5%BCywania-rurek-tracheostomijnych-produkcji
  • 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
    Announcement of the company Pyramed Sp. z o. o. suspension of the marketing and use of tracheostomy tubes produced by JiangsuKaishou Medical Apparatus (10/09/2009)
Notificaciones De Seguridad De Campo acerca de three-wire taps with a drain, series 12.01.2009
  • Tipo de evento
    Field Safety Notice
  • ID del evento
    2522
  • Fecha
    2009-10-02
  • País del evento
    Poland
  • Fuente del evento
    ORMPMDBP
  • URL de la fuente del evento
    http://www.urpl.gov.pl/pl/komunikat-firmy-romed-medical-dotycz%C4%85cy-wycofania-tr%C3%B3jprzewodowych-kranik%C3%B3w-z-drenem-serii-12012009
  • 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
    ROMED-MEDICAL message regarding the withdrawal of three-wire taps with a drain, series 12.01.2009 (02/10/2009)
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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.