Alerta De Seguridad para G4 PLATINUM and Dexcom G5 Mobile receiver

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

¿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
    2016-03-09
  • Fecha de publicación del evento
    2016-03-09
  • 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: dexcom g4 platinum and dexcom g5 mobile receiver the therapeutic goods administration (tga) of australia has posted a medical device safety alert concerning dexcom g4 platinum and dexcom g5 mobile receiver manufactured by dexcom incorporated. [part number: mt20649-2 and mt22719-2]. the manufacturer has noticed an increase in complaints related to audible alarms and alerts associated with dexcom g4 platinum and dexcom g5 receivers while monitoring product complaints through their quality management system. the manufacturer is notifying all affected customers that they may not receive an intended audible alarm or alert. as a result, if they rely on hearing the alarm or alert, they may not detect a severe hypoglycaemic (low glucose) or hyperglycaemic (high glucose) event. this includes the fixed low alarm at 3.1 mmol/l, which alerts the user with vibration first, followed by beeps 5 minutes later if not confirmed. the vibration alert should continue to work; however, the audible beeps may not function. the vibration function for the alerts and alarm cannot be disabled by the user. the manufacturer is providing users with instructions on how to test the audible alarms to ensure they are functioning properly. according to the local supplier, dexcom g4 platinum is distributed in hong kong but not dexcom g5 mobile receiver. for details, please refer to the tga website: http://apps.Tga.Gov.Au/prod/sara/arn-detail.Aspx?k=rc-2016-rn-00224-1 if you are in possession of the affected product, please contact your supplier for necessary actions. posted on 9 march 2016.

Device

  • Modelo / Serial
  • Descripción del producto
    Medical Device Safety Alert: Dexcom G4 PLATINUM and Dexcom G5 Mobile receiver
  • Manufacturer

Manufacturer