Alerta De Seguridad para Defibrillator/pacer SLIM corpuls3

Según Department of Health, este evento ( alerta de seguridad ) involucró a un dispositivo médico en Hong Kong que fue producido por Device Technologies.

¿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
  • Fecha
    2014-09-17
  • Fecha de publicación del evento
    2014-09-17
  • País del evento
  • Fuente del evento
    DH
  • URL de la fuente del evento
  • Notas / Alertas
    Hong Kong data is current through September 2018. All of the data comes from the Department of Health (Hong Kong), 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 Hong Kong.
  • Notas adicionales en la data
    Medical Device Safety Alert
  • Causa
    Medical device safety alert: device technologies defibrillator/pacer slim corpuls3 the australia therapeutic goods administration (tga) posted a medical device safety alert concerning defibrillator/pacer slim corpuls3 (product code: cp-4301) manufactured by device technologies. according to the alert, there is the possibility that a component on that circuit board could be damaged mechanically due to too little distance between a circuit board and the housing. this impairs the radio connection between the modules. the user can recognise this, if a respective error message (ie. “no connection to defibrillator unit” or “no connection to p-box”) is displayed. in rare cases this can result in impairment of the radio connection between the modules, and then it is no longer possible to: a) perform full patient monitoring; and b) correctly adjust and operate a therapy function of the device. vibrations have been found to increase the likelihood of this malfunction. due to this issue, diagnosis and therapy are delayed, because the measurement and therapy functions cannot perform without problems. the manufacturer is advising the customer to connect the module mechanically to form a compact device if the error message is displayed. a permanent correction of the error is only possible by replacing the affected radio module. the manufacturer is arranging replacement of the radio module. for details, please refer to tga website http://www.Tga.Gov.Au/sara/arn-detail.Aspx?k=rc-2014-rn-00979-1 if you are in possession of the product, please contact your supplier for necessary actions. posted on 17 september 2014.

Device

  • Modelo / Serial
  • Descripción del producto
    Medical Device Safety Alert: Device Technologies Defibrillator/pacer SLIM corpuls3
  • Manufacturer

Manufacturer