Alerta De Seguridad para Heartstart MRx Defibrillator, Philips brand, model: M3535A, M3536A, Registro ANVISA: 10216710136

Según Agência Nacional de Vigilância Sanitária (ANVISA), este evento ( alerta de seguridad ) involucró a un dispositivo médico en Brazil que fue producido por Philips Medical Systems.

¿Qué es esto?

Las alertas proporcionan información importante y recomendaciones sobre los productos. Aunque se haya emitido una alerta, esto no significa necesariamente que el producto se considera peligroso. Las alertas de seguridad, dirigidas a trabajadores de la salud y a usuarios, pueden incluir retiro de equipos. Pueden ser escritas por los fabricantes, pero también por funcionarios del área de salud.

Más información acerca de la data acá
  • Tipo de evento
    Safety alert
  • ID del evento
    1362
  • Fecha
    2014-02-14
  • País del evento
  • Fuente del evento
    ANVISA
  • URL de la fuente del evento
  • Notas / Alertas
    Brazilian data is current through June 2018. All of the data comes from Anvisa, 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 data from the U.S. and Brazil.
  • Notas adicionales en la data
    When monitoring through ECG electrodes, there is a potential for: • Loss of stimulation demand mode • Inability to perform synchronized cardioversion with blades • Interruption of ECG monitoring You can continue to use the MRx before installing the update of the hardware being aware that if this problem occurs, you may experience the following symptoms: • Loss of stimulation demand mode • Inability to perform synchronized cardioversion with blades • Interruption of ECG monitoring or INOP messages If these problems occur, consult the HeartStart MRx Instructions for Use for troubleshooting assistance. In addition, the following measures can be taken: • If pacing demand mode is not available, fixed pacing mode can be used. Change the pacing mode to "fixed" in the pacing mode menu. • If synchronized cardioversion with the blades is not available, synchronized cardioversion with blades can be used. Switch to blades • If monitoring of ECG electrodes is not available, ECG monitoring via blades / blades is available. Plug the blade or paddle cable and push the branch selector button until the ECG waves from the blades or blades are displayed. • Connect a separate ECG trunk cable, if available. Important Note: Defibrillation, fixed pacing mode, paddle / paddle ECG monitoring, and other monitoring functions are not affected by this problem.
  • Causa
    The connection of the ecg trunk cable and the locking of the mrx connector may be subject to accelerated wear, which may result in an uninterrupted ecg signal. interruption of the ecg signal may cause: • loss of stimulation demand mode • inability to perform synchronized cardioversion with the paddles • interruption of monitoring of ecg leads, which may delay appropriate treatment defibrillation, fixed pacing mode , paddle / paddle ecg monitoring, and other monitoring functions are not affected by this problem.
  • Acción
    field correction and software update

Manufacturer

  • Empresa matriz del fabricante (2017)
  • Source
    ANVSANVISA