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  • Dispositivo 1149
  • Fabricante 31827
  • Evento 1201
  • Implante 0
Gambro Renal Products
  • Empresa matriz del fabricante (2017)
    Baxter International
  • Source
    MHM
Microm International GmbH
  • Empresa matriz del fabricante (2017)
    Thermo Fisher Scientific Inc
  • Source
    MHM
BD
  • Empresa matriz del fabricante (2017)
    Becton, Dickinson and Company
  • Source
    MHM
Thoratec Corporation
  • Empresa matriz del fabricante (2017)
    Abbott Laboratories
  • Comentario del fabricante
    “We are in constant communication with regulatory agencies and competent authorities worldwide which allows us to implement global recalls or in-country communication quickly and effectively,” Abbott, which now owns St. Jude Medical told ICIJ in a statement. In addition to sending global notices to physicians worldwide, we also make sure that product advisories are available online and classification of product recalls and product advisories are determined by global regulatory bodies which can impact the timing in any given country. MD companies follow varying regulations in different countries. In come countries software is not regulated so a recall in one country related to software would not be classified as a recall or field action in another. In addition, review cycles within the regulatory process can be different in each country which can impact communication and recall timing.
  • Source
    MHM
GlaxoSmithKline
  • Empresa matriz del fabricante (2017)
    Glaxosmithkline Plc
  • Source
    MHM
Fisher & Paykel Healthcare
  • Empresa matriz del fabricante (2017)
    Fisher & Paykel Healthcare Corporation Limited
  • Source
    MHM
Guangzhou Wondfo Biotech Co. Ltd.
  • Empresa matriz del fabricante (2017)
    Guangzhou Wondfo Biotech Co. Ltd.
  • Source
    MHM
Arrow International Inc
  • Empresa matriz del fabricante (2017)
    Teleflex Incorporated
  • Source
    MHM
ConMed Linvatec
  • Empresa matriz del fabricante (2017)
    CONMED Corp.
  • Source
    MHM
Exelint International Inc
  • Empresa matriz del fabricante (2017)
    Exelint International Co.
  • Source
    MHM
RECKITT BENCKISER
  • Empresa matriz del fabricante (2017)
    Reckitt Benckiser Group Plc
  • Source
    MHM
Medtronic International Ltd.
  • Empresa matriz del fabricante (2017)
    Medtronic plc
  • Comentario del fabricante
    “If our surveillance systems identify a potential performance issue, our personnel promptly evaluate the problem, including, when appropriate, conducting root cause investigations and internal testing to assess whether the product continues to meet specifications and defined performance criteria,” Medtronic told ICIJ in a statement. “In some cases, based on this evaluation, Medtronic may determine that a recall is necessary.” The company said that it communicates with healthcare providers and/or patients and provide recommendations to address such issues. Medtronic noted that these communications can include letters, emails, calls, press releases, physician notifications and social media postings, as well as informing the FDA and other regulators of the actions.
  • Source
    MHM
P3 Medical Ltd company
  • Empresa matriz del fabricante (2017)
    Jardines (U.K.) Limited
  • Source
    MHM
ev3 Limited
  • Empresa matriz del fabricante (2017)
    Medtronic plc
  • Comentario del fabricante
    “If our surveillance systems identify a potential performance issue, our personnel promptly evaluate the problem, including, when appropriate, conducting root cause investigations and internal testing to assess whether the product continues to meet specifications and defined performance criteria,” Medtronic told ICIJ in a statement. “In some cases, based on this evaluation, Medtronic may determine that a recall is necessary.” The company said that it communicates with healthcare providers and/or patients and provide recommendations to address such issues. Medtronic noted that these communications can include letters, emails, calls, press releases, physician notifications and social media postings, as well as informing the FDA and other regulators of the actions.
  • Source
    MHM
Johnson & Johnson Vision Care
  • Empresa matriz del fabricante (2017)
    Johnson & Johnson
  • Source
    MHM
Becton Dickinson & Co.
  • Empresa matriz del fabricante (2017)
    Becton, Dickinson and Company
  • Source
    MHM
Hospira, Inc.
  • Empresa matriz del fabricante (2017)
    Pfizer
  • Source
    MHM
Advanced Bionics Llc
  • Empresa matriz del fabricante (2017)
    Sonova Holding Ag
  • Source
    MHM
Respironics Inc.
  • Empresa matriz del fabricante (2017)
    Philips
  • Source
    MHM
Levitronix, Inc.
  • Empresa matriz del fabricante (2017)
    Levitronix Gmbh
  • Source
    MHM
Siemens Medical Solutions
  • Empresa matriz del fabricante (2017)
    Siemens Ag
  • Source
    MHM
Cook, Inc.
  • Empresa matriz del fabricante (2017)
    Medtronic plc
  • Comentario del fabricante
    “If our surveillance systems identify a potential performance issue, our personnel promptly evaluate the problem, including, when appropriate, conducting root cause investigations and internal testing to assess whether the product continues to meet specifications and defined performance criteria,” Medtronic told ICIJ in a statement. “In some cases, based on this evaluation, Medtronic may determine that a recall is necessary.” The company said that it communicates with healthcare providers and/or patients and provide recommendations to address such issues. Medtronic noted that these communications can include letters, emails, calls, press releases, physician notifications and social media postings, as well as informing the FDA and other regulators of the actions.
  • Source
    MHM
Defibtech LLC
  • Empresa matriz del fabricante (2017)
    Nihon Kohden Corp.
  • Source
    MHM
INO THERAPEUTICS
  • Empresa matriz del fabricante (2017)
    Mallinckrodt Plc
  • Source
    MHM
ConMed Corporation
  • Empresa matriz del fabricante (2017)
    CONMED Corp.
  • Source
    MHM
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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.