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  • Dispositivo 2677
  • Fabricante 2677
  • Evento 2803
  • Implante 0
Notificaciones De Seguridad De Campo acerca de tracheostomy tubes
  • Tipo de evento
    Field Safety Notice
  • ID del evento
    1152
  • Fecha
    2007-03-08
  • País del evento
    Poland
  • Fuente del evento
    ORMPMDBP
  • URL de la fuente del evento
    http://www.urpl.gov.pl/pl/rurki-tracheostomijne-produkcji-unomedical-decyzja-nr-dwmnr032007-08032007
  • 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
    Tracheostomy tubes produced by UNOMEDICAL - Decision no. D / WM / NR / 03/2007 (08.03.2007)
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 infusion pumps
  • Tipo de evento
    Field Safety Notice
  • ID del evento
    2437
  • Fecha
    2007-03-20
  • País del evento
    Poland
  • Fuente del evento
    ORMPMDBP
  • URL de la fuente del evento
    http://www.urpl.gov.pl/pl/pompy-infuzyjne-produkcji-kwapisz-pompy-infuzyjne-decyzja-nr-dwmnr042007-20032007
  • 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
    Infusion pumps manufactured by "KWAPISZ-POMPY INFUZYJNE" - Decision no. D / WM / NR / 04/2007 (20.03.2007)
Notificaciones De Seguridad De Campo acerca de infusion pumps
  • Tipo de evento
    Field Safety Notice
  • ID del evento
    1720
  • Fecha
    2007-03-20
  • País del evento
    Poland
  • Fuente del evento
    ORMPMDBP
  • URL de la fuente del evento
    http://www.urpl.gov.pl/pl/pompy-infuzyjne-produkcji-kwapisz-pompy-infuzyjne-decyzja-nr-dwmnr062007-20032007
  • 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
    Infusion pumps manufactured by "KWAPISZ-POMPY INFUZYJNE" - Decision No. D / WM / NR / 06/2007 (20.03.2007)
Notificaciones De Seguridad De Campo acerca de infusion pumps
  • Tipo de evento
    Field Safety Notice
  • ID del evento
    1671
  • Fecha
    2007-03-20
  • País del evento
    Poland
  • Fuente del evento
    ORMPMDBP
  • URL de la fuente del evento
    http://www.urpl.gov.pl/pl/pompy-infuzyjne-produkcji-kwapisz-pompy-infuzyjne-decyzja-nr-dwmnr052007-20032007
  • 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
    Infusion pumps produced by "KWAPISZ-POMPY INFUZYJNE" - Decision No. D / WM / NR / 05/2007 (20.03.2007)
Notificaciones De Seguridad De Campo acerca de infusion pumps
  • Tipo de evento
    Field Safety Notice
  • ID del evento
    1779
  • Fecha
    2007-03-21
  • País del evento
    Poland
  • Fuente del evento
    ORMPMDBP
  • URL de la fuente del evento
    http://www.urpl.gov.pl/pl/pompy-infuzyjne-produkcji-kwapisz-pompy-infuzyjne-notatka-doradcza-21032007
  • 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
    Infusion pumps manufactured by "KWAPISZ-POMPY INFUZYJNE" - Advisory note (21.03.2007)
Notificaciones De Seguridad De Campo acerca de infusion pumps
  • Tipo de evento
    Field Safety Notice
  • ID del evento
    1225
  • Fecha
    2007-03-21
  • País del evento
    Poland
  • Fuente del evento
    ORMPMDBP
  • URL de la fuente del evento
    http://www.urpl.gov.pl/pl/pompy-infuzyjne-produkcji-kwapisz-pompy-infuzyjne-notatka-doradcza-21032007-0
  • 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
    Infusion pumps manufactured by "KWAPISZ-POMPY INFUZYJNE" - Advisory note (21.03.2007)
Notificaciones De Seguridad De Campo acerca de lumbar spinal needles spinal needle whitacare penc...
  • Tipo de evento
    Field Safety Notice
  • ID del evento
    1976
  • Fecha
    2007-04-24
  • 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-do-nak%C5%82u%C4%87-l%C4%99d%C5%BAwiowych-spinal-needle-whitacare-pencil-point-24042007
  • 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 regarding lumbar spinal needles Spinal Needle Whitacare Pencil Point (24/04/2007)
Notificaciones De Seguridad De Campo acerca de bioenergy-electro-photon-thermodynamic mattresses ...
  • Tipo de evento
    Field Safety Notice
  • ID del evento
    2246
  • Fecha
    2007-06-01
  • País del evento
    Poland
  • Fuente del evento
    ORMPMDBP
  • URL de la fuente del evento
    http://www.urpl.gov.pl/pl/decyzja-o-wycofaniu-z-obrotu-materacy-bioenergo-elektromagneto-fotono-termodynamicznych-beft-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
    Decision on the withdrawal from the market of bioenergy-electro-photon-thermodynamic mattresses BEFT (01/06/2007)
Notificaciones De Seguridad De Campo acerca de bioenergy-electro-photon-thermodynamic mattresses ...
  • Tipo de evento
    Field Safety Notice
  • ID del evento
    2485
  • Fecha
    2007-06-01
  • País del evento
    Poland
  • Fuente del evento
    ORMPMDBP
  • URL de la fuente del evento
    http://www.urpl.gov.pl/pl/decyzja-o-wycofaniu-z-obrotu-materacy-bioenergo-elektromagneto-fotono-termodynamicznych-beft
  • 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
    Decision on the withdrawal from the market of bioenergy-electro-photon-thermodynamic mattresses BEFT (01/06/2007)
Notificaciones De Seguridad De Campo acerca de catheters foley
  • Tipo de evento
    Field Safety Notice
  • ID del evento
    2483
  • Fecha
    2007-06-13
  • País del evento
    Poland
  • Fuente del evento
    ORMPMDBP
  • URL de la fuente del evento
    http://www.urpl.gov.pl/pl/decyzja-o-wycofaniu-z-obrotu-i-z-u%C5%BCywania-na-terytorium-rzeczypospolitej-polskiej-wszystkich-serie
  • 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
    Decision to withdraw from circulation and use on the territory of the Republic of Poland all series of medical devices catheters Foley (13.06.2007)
Notificaciones De Seguridad De Campo acerca de Surgical clothing, non-reusable, reusable; Surgica...
  • Tipo de evento
    Field Safety Notice
  • ID del evento
    2469
  • Fecha
    2007-06-19
  • País del evento
    Poland
  • Fuente del evento
    ORMPMDBP
  • URL de la fuente del evento
    http://www.urpl.gov.pl/pl/decyzja-o-wstrzymaniu-wprowadzenia-do-obrotu-wyrob%C3%B3w-firmy-carima-19062007
  • 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
    Decision to suspend the introduction of CARIMA's products (19.06.2007)
Notificaciones De Seguridad De Campo acerca de surgical apron, surgical drapes, medical rubber pa...
  • Tipo de evento
    Field Safety Notice
  • ID del evento
    2733
  • Fecha
    2007-06-19
  • País del evento
    Poland
  • Fuente del evento
    ORMPMDBP
  • URL de la fuente del evento
    http://www.urpl.gov.pl/pl/decyzja-o-wstrzymaniu-wprowadzenia-do-obrotu-wyrob%C3%B3w-firmy-medyk-pol-19062007
  • 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
    Decision to suspend the introduction of MEDYK-POL products on the market (19.06.2007)
Notificaciones De Seguridad De Campo acerca de Surgeon's coat, non-sterile, reusable; Surgical cl...
  • Tipo de evento
    Field Safety Notice
  • ID del evento
    1422
  • Fecha
    2007-06-19
  • País del evento
    Poland
  • Fuente del evento
    ORMPMDBP
  • URL de la fuente del evento
    http://www.urpl.gov.pl/pl/decyzja-o-wstrzymaniu-wprowadzenia-do-obrotu-wyrob%C3%B3w-firmy-dorex-19062007
  • 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
    Decision to suspend the introduction of DOREX products (19.06.2007)
Notificaciones De Seguridad De Campo acerca de contact lens care
  • Tipo de evento
    Field Safety Notice
  • ID del evento
    2702
  • Fecha
    2007-06-28
  • País del evento
    Poland
  • Fuente del evento
    ORMPMDBP
  • URL de la fuente del evento
    http://www.urpl.gov.pl/pl/komunikat-o-wycofaniu-p%C5%82ynu-do-piel%C4%99gnacji-soczewek-kontaktowych-28062007
  • 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 regarding the withdrawal of contact lens care (June 28, 2007)
Notificaciones De Seguridad De Campo acerca de CS3000
  • Tipo de evento
    Field Safety Notice
  • ID del evento
    2123
  • Fecha
    2007-07-05
  • País del evento
    Poland
  • Fuente del evento
    ORMPMDBP
  • URL de la fuente del evento
    http://www.urpl.gov.pl/pl/komunikat-o-wycofaniu-zestawu-do-aferezy-cs3000-firmy-baxter-05072007
  • 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 about withdrawal of the BAXTER CS3000 apheresis kit (05.07.2007)
Notificaciones De Seguridad De Campo acerca de clearstar enteral pumps
  • Tipo de evento
    Field Safety Notice
  • ID del evento
    1622
  • Fecha
    2007-07-16
  • País del evento
    Poland
  • Fuente del evento
    ORMPMDBP
  • URL de la fuente del evento
    http://www.urpl.gov.pl/pl/infromacja-dotycz%C4%85ca-pomp-clearstar-enteral-16072007
  • 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 ClearStar Enteral pumps (July 16, 2007)
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 kd-fine needles
  • Tipo de evento
    Field Safety Notice
  • ID del evento
    2198
  • Fecha
    2007-08-10
  • País del evento
    Poland
  • Fuente del evento
    ORMPMDBP
  • URL de la fuente del evento
    http://www.urpl.gov.pl/pl/powiadomienia-z-firmy-intergos-w-sprawie-igie%C5%82-kd-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
    Notifications from Intergos regarding needles KD-Fine (10/08/2007)
Notificaciones De Seguridad De Campo acerca de disposable syringes with a capacity of 2, 5, 10ml
  • Tipo de evento
    Field Safety Notice
  • ID del evento
    1304
  • Fecha
    2007-08-23
  • País del evento
    Poland
  • Fuente del evento
    ORMPMDBP
  • URL de la fuente del evento
    http://www.urpl.gov.pl/pl/komunikat-w-sprawie-strzykawek-jednorazowych-o-pojemno%C5%9Bci-2-5-10ml-23082007
  • 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 regarding disposable syringes with a capacity of 2, 5, 10ml (23/08/2007)
Notificaciones De Seguridad De Campo acerca de minimed paradigm insulin pumps
  • Tipo de evento
    Field Safety Notice
  • ID del evento
    2549
  • Fecha
    2007-08-27
  • País del evento
    Poland
  • Fuente del evento
    ORMPMDBP
  • URL de la fuente del evento
    http://www.urpl.gov.pl/pl/informacja-dotycz%C4%85ca-pomp-insulinowych-minimed-paradigm-27082007
  • 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 MiniMed Paradigm insulin pumps (27/08/2007)
Notificaciones De Seguridad De Campo acerca de blood transfusion devices
  • Tipo de evento
    Field Safety Notice
  • ID del evento
    2353
  • Fecha
    2007-08-31
  • País del evento
    Poland
  • Fuente del evento
    ORMPMDBP
  • URL de la fuente del evento
    http://www.urpl.gov.pl/pl/komunikat-w-sprawie-przyrz%C4%85d%C3%B3w-do-przetaczania-krwi-produkcji-weigao-group-medical-31082007
  • 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
    Communiqué on Weigao Group Medical blood transfusion devices (August 31, 2007)
Notificaciones De Seguridad De Campo acerca de blood transfusion devices and devices for infusion...
  • Tipo de evento
    Field Safety Notice
  • ID del evento
    1444
  • Fecha
    2007-09-03
  • País del evento
    Poland
  • Fuente del evento
    ORMPMDBP
  • URL de la fuente del evento
    http://www.urpl.gov.pl/pl/komunikat-firmy-margomed-w-sprawie-przyrz%C4%85d%C3%B3w-do-przetaczania-krwi-oraz-przyrz%C4%85d%C3%B3w-do-podawania
  • 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
    Margomed's announcement regarding blood transfusion devices and devices for administering infusion fluids (03/09/2007)
Notificaciones De Seguridad De Campo acerca de 0.65oz / 18m toothpaste
  • Tipo de evento
    Field Safety Notice
  • ID del evento
    1497
  • Fecha
    2007-09-14
  • País del evento
    Poland
  • Fuente del evento
    ORMPMDBP
  • URL de la fuente del evento
    http://www.urpl.gov.pl/pl/komunikat-w-sprawie-wycofania-przez-firm%C4%99-gilchrist-soames-pasty-do-z%C4%99b%C3%B3w-065oz18m-14092007
  • 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 regarding the withdrawal of 0.65oz / 18m toothpaste by Gilchrist & Soames. (14.09.2007)
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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.