Alerta De Seguridad para cobas taqscreen mpx test, version 2.0

Según Department of Health, este evento ( alerta de seguridad ) involucró a un dispositivo médico en Hong Kong que fue producido por Roche Molecular 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
  • Fecha
    2012-10-25
  • Fecha de publicación del evento
    2012-10-25
  • 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: roche cobas taqscreen mpx test, version 2.0 the medicines and healthcare products regulatory agency (mhra), united kingdom posted a field safety notice concerning cobas taqscreen mpx test, version 2.0, manufactured by roche molecular systems, inc. according to the manufacturer, the package insert, part no. 05969492190, v.2.0, used with the cobas taqscreen mpx test, version 2.0 for use on the cobas s 201 system, ce-ivd contains incorrect specimen transport stability parameters. the living donor specimen transport stability claim in the specimen collection, storage and handling section of the cobas taqscreen mpx test, version 2.0 ce package insert currently allows users to store blood collected in edta, cpd, cpda1 or cp2d for up to 72 hours at 2-30 °c. the package insert will be revised to inform users that blood collected in edta, cpd, cpda1 or cp2d can only be stored for up to 48 hours at 2-25 °c. the manufacturer advised users to immediately take the following actions: users should begin using the new specimen transport conditions as below: blood collected in edta may be stored for up to 48 hours at 2 - 25°c. blood collected in cpd, cpda1 or cp2d may be stored for up to 48 hours at 2 - 25°c. whole blood samples with hcv titers near 20.4 iu/ml or lower stored under conditions stated above, should be reviewed, as, although unlikely, they possibly could have been impacted by this issue. furthermore, product labeling will be updated with the next kit build by the manufacturer. for details, please refer to mhra website: http://www.Mhra.Gov.Uk/safetyinformation/safetywarningsalertsandrecalls/fieldsafetynotices/con195873 if you are in possession of the affected product, please contact your supplier for necessary actions. posted on 25 october 2012.

Device

  • Modelo / Serial
  • Descripción del producto
    Medical Device Safety Alert: Roche Cobas TaqScreen MPX Test, version 2.0
  • Manufacturer

Manufacturer