Events

Retiro De Equipo (Recall) de CAPNOSTREAM20P ROHS COMPLIANT

Según Health Canada (via FOI), este evento ( retiro de equipo (recall) ) involucró a un dispositivo médico en Canada que fue producido por COVIDIEN.

¿Qué es esto?

Una corrección al equipo o acción de retiro tomada por el fabricante para abordar un problema con un dispositivo médico. Los retiros (recalls) ocurren cuando un dispositivo médico está defectuoso, cuando puede poner en riesgo la salud, o cuando simultáneamente está defectuoso y puede poner en riesgo la salud.

Más información acerca de la data acá
  • Tipo de evento
    Recall
  • ID del evento
    24299
  • Clase de Riesgo del Evento
    I
  • Fecha de inicio del evento
    2016-04-20
  • País del evento
    Canada
  • Fuente del evento
    HC
  • Notas / Alertas
    Canadian data is current through March 2018. All of the data comes from Health Canada, 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 Canada.
  • Notas adicionales en la data
  • Causa
    This voluntary recall is due to a supplier defect in battery manufacturing that may increase the risk of thermal damage to the battery pack. medtronic has received seven reports of thermal damage out of 9817 battery packs. of these seven reports one involved a fire resulting in smoke inhalation and minor burns.

Device

CAPNOSTREAM20P ROHS COMPLIANT
  • Modelo / Serial
    Model Catalog: CS08657-02 (Lot serial: >10 CONTACT MFR); Model Catalog: CS08657-01 (Lot serial: >10 CONTACT MFR); Model Catalog: CS08651-01 (Lot serial: >10 CONTACT MFR); Model Catalog: CS08651-02 (Lot serial: >10 CONTACT MFR); Model Catalog: 016400 (Lot serial: >10 CONTACT MFR)
  • Clasificación del producto
    Anesthesiology Devices
  • Descripción del producto
    CAPNOSTREAM20P ROHS COMPLIANT;CAPNOSTREAM20P NELLCOR MODEL;CAPNOSTREAM BATTERY PACK
  • Manufacturer
    COVIDIEN

Manufacturer

COVIDIEN
  • Dirección del fabricante
    SAINT-LAURENT
  • 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