Alerta De Seguridad para Monitor/ Defibrillator DEFIGARD Touch7

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

¿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
    2018-01-30
  • Fecha de publicación del evento
    2017-01-30
  • 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: schiller medical, monitor/ defibrillator defigard touch7 the health sciences authority (hsa), singapore posted a medical device safety alert concerning monitor/ defibrillator defigard touch7 [all devices with software version up to “soft 5” are affected]. the defigard touch7 can be configured in 3 different start modes (monitoring, aed or manual defibrillator). the field safety notice concerns devices configured in start mode “manual defibrillator’. if the user starts the device in this configuration, and switches directly from the manual defibrillation to the synchronized defibrillation mode, without ecg patient cable being plugged, then the device will be unable to trigger the synchronized defibrillation shock. this can be seen on the screen of the device, no trigger pulses are available. if the patient cable is connected, according to the user manual, this failure does not occur. according to the manufacturer, it may be unable to perform synchronized defibrillation therapy. the manual defibrillation mode at start is a specific medical emergency service setting. it is used when rescuer wants to mainly use the device as manual defibrillator. the synchronized defibrillation is not an emergency procedure, and it is recommended to perform it with ecg patient cable. while waiting for the update of the defigard touch 7, affected users are advised to continue to use it without restriction. if user startup configuration with manual defibrillation mode, user has to select another startup mode, until the update to software “soft 6”, or use a patient cable for the synchronized defibrillation therapy, as described in the user manual. for details, please visit the following hsa website: http://www.Hsa.Gov.Sg/content/dam/hsa/hprg/medical_devices/updates_and_safety_reporting/field_safety_corrective_action/fsn/2017/november/hsa%206004101-056-17-06_36%20fsn_redacted.Pdf if you are in possession of the affected products, please contact your supplier for necessary actions. posted on 30 january 2017.

Device

  • Modelo / Serial
  • Descripción del producto
    Medical Device Safety Alert: Schiller Medical, Monitor/ Defibrillator DEFIGARD Touch7
  • Manufacturer

Manufacturer