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  • Dispositivo 13259
  • Fabricante 13259
  • Evento 13553
  • Implante 0
MEDTRONIC OF CANADA LTD.
  • Dirección del fabricante
    BRAMPTON
  • 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
    HC
SMITH & NEPHEW INC.
  • Dirección del fabricante
    MISSISSAUGA
  • Empresa matriz del fabricante (2017)
    Smith & Nephew plc
  • Source
    HC
SIEMENS HEALTHCARE LIMITED
  • Dirección del fabricante
    OAKVILLE
  • Empresa matriz del fabricante (2017)
    Siemens Ag
  • Source
    HC
LIKO CARE
  • Dirección del fabricante
    NORBATTEN
  • Source
    HC
INVACARE CORPORATION
  • Dirección del fabricante
    ELYRIA
  • Empresa matriz del fabricante (2017)
    Invacare Corporation
  • Source
    HC
PHILIPS ELECTRONICS LTD.
  • Dirección del fabricante
    MARKHAM
  • Empresa matriz del fabricante (2017)
    Philips
  • Source
    HC
MEDTRONIC OF CANADA LTD.
  • Dirección del fabricante
    BRAMPTON
  • 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
    HC
BECTON DICKINSON CANADA INC.
  • Dirección del fabricante
    MISSISSAUGA
  • Empresa matriz del fabricante (2017)
    Becton, Dickinson and Company
  • Source
    HC
MEDI-MAN REHABILITATION PRODUCTS INC.
  • Dirección del fabricante
    MISSISSAUGA
  • Source
    HC
MEDTRONIC OF CANADA LTD.
  • Dirección del fabricante
    BRAMPTON
  • 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
    HC
MEDTRONIC OF CANADA LTD.
  • Dirección del fabricante
    BRAMPTON
  • 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
    HC
BARD CANADA INC.
  • Dirección del fabricante
    OAKVILLE
  • Empresa matriz del fabricante (2017)
    Becton, Dickinson and Company
  • Source
    HC
INVERNESS MEDICAL CANADA
  • Dirección del fabricante
    OTTAWA
  • Source
    HC
NOVA CENTURY SCIENTIFIC INC. A DIVISION OF TRINITY BIOTECH PLC.
  • Dirección del fabricante
    BURLINGTON
  • Empresa matriz del fabricante (2017)
    Trinity Biotech plc
  • Source
    HC
ROCHE DIAGNOSTICS CORPORATION
  • Dirección del fabricante
    INDIANAPOLIS
  • Source
    HC
CARDINAL HEALTH CANADA
  • Dirección del fabricante
    VAUGHAN
  • Empresa matriz del fabricante (2017)
    Cardinal Health
  • Source
    HC
SIEMENS CANADA LIMITED - HEALTHCARE
  • Dirección del fabricante
    MISSISSAUGA
  • Empresa matriz del fabricante (2017)
    Siemens Ag
  • Source
    HC
VARIAN MEDICAL SYSTEMS INC.
  • Dirección del fabricante
    PALO ALTO
  • Empresa matriz del fabricante (2017)
    Varian Medical Systems Inc
  • Source
    HC
MIZUHO CORPORATION
  • Dirección del fabricante
    TOKYO
  • Source
    HC
CARDINAL HEALTH CANADA INC.
  • Dirección del fabricante
    MISSISSAUGA
  • Empresa matriz del fabricante (2017)
    Cardinal Health
  • Source
    HC
SIEMENS CANADA LIMITED - HEALTHCARE
  • Dirección del fabricante
    MISSISSAUGA
  • Empresa matriz del fabricante (2017)
    Siemens Ag
  • Source
    HC
RANDOX LABORATORIES LTD.
  • Dirección del fabricante
    CRUMLIN
  • Empresa matriz del fabricante (2017)
    Randox Holdings Limited
  • Source
    HC
CARDINAL HEALTH CANADA INC.
  • Dirección del fabricante
    MISSISSAUGA
  • Empresa matriz del fabricante (2017)
    Cardinal Health
  • Source
    HC
SMITH & NEPHEW INC.
  • Dirección del fabricante
    MISSISSAUGA
  • Empresa matriz del fabricante (2017)
    Smith & Nephew plc
  • Source
    HC
E I DUPONT DE NEMOURS & CO INC
  • Dirección del fabricante
    DELAWARE
  • Source
    HC
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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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