Notificaciones De Seguridad De Campo acerca de ONLINE TDM Gentamicin assay

Según Agency for Medicinal Products and Medical Devices of the Republic of Slovenia (via FOI), este evento ( notificaciones de seguridad de campo ) involucró a un dispositivo médico en Slovenia que fue producido por Roche Diagnostics.

¿Qué es esto?

Las notificaciones de seguridad de campo son comunicaciones sobre acciones que se pueden estar tomando en relación con un producto que se encuentra en el mercado, enviadas por los fabricantes de dispositivos médicos o sus representantes. Estas notificaciones son principalmente para trabajadores de la salud, pero también para usuarios. Pueden incluir alertas y retiro de equipos.

Más información acerca de la data acá
  • Tipo de evento
    Field Safety Notice
  • País del evento
  • Fuente del evento
    AMPMDRS
  • Notas / Alertas
    Data from Slovenia is current through February 2019. All of the data comes from the Agency for Medicinal Products and Medical Devices of the Republic of Slovenia (via FOI), 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 Slovenia.
  • Notas adicionales en la data
  • Causa
    In the last version of this customer letter we informed you about the implementation of an instrument factor (if) for online tdm gentamicin that was - based on available data - the mitigation for the reported issue. however, against initial data the correction of the instrument factor did not mitigate the issue. we received complaints from customers who implemented the if, observing decreased sample recovery using the online tdm gentamicin assay. since availability of fresh patient samples for gentamicin is very limited, frozen patient samples had to be used for internal investigations. obviously, the internal results obtained with these samples and used for the implementation of the if did not match with the external observations reported by customers. further investigations were initiated at roche to understand this mismatch. in order to verify the internal results a new panel of patient samples was collected (panel b, stored at -80°c) and compared to the panel that was used for the determination of the if (panel a, stored at -20°c). .

Device

  • Modelo / Serial
    04490843190 ONLINE TDM Gentamicin 100 Tests c 311, c 501/502 05841291190 ONLINE TDM Gentamicin 100 Tests c 701/702
  • Manufacturer

Manufacturer