Alerta De Seguridad para FRED easy & FRED easy Life Defibrillators

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

¿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
    2012-05-22
  • Fecha de publicación del evento
    2012-05-22
  • 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 fred easy & fred easy life defibrillators the medicines and healthcare products regulatory agency (mhra), united kingdom posted a field safety notice concerning fred easy & fred easy life defibrillators manufactured by schiller medical. according to schiller medical, two problems have been identified regarding “transistor charge error” message and quality of the electrodes. transistor charge error: on some devices, during use, or during a self test, a message “transistor charge error” has occurred. in the analysed cases (field and laboratory results), all occurrences were “false positive”, the devices were not affected by a failure. as a consequence, the device is unavailable until it is restarted. the occurrence of the failure is estimated to 0.2%. the corrective action consists in a software update, which prevents the occurrence of the “false positive”. electrodes: a decline in the quality, before expiry date, has been observed for some schiller electrodes manufactured by nessler (p/n 0-21-0000, 0-21-0003, 0-21-0020, 0-21-0021, 0-21-0013, 0-21-0024, 2.155056, 2.155057, w1410241, w1404262). the consequences were a decrease of survival chances for some patients, due to the lack of heart rhythm analysis. all schiller electrodes which are still on the market, with a valid expiry date and manufactured by nessler, will be exchanged by new schiller electrodes manufactured by leonhard lang. according to the local supplier, the affected products have been distributed in hong kong. for details, please refer to the following mhra website: http://www.Mhra.Gov.Uk/safetyinformation/safetywarningsalertsandrecalls/fieldsafetynotices/index.Htm if you are in possession of the affected products, please contact your supplier for necessary actions. posted 22 may 2012.

Device

  • Modelo / Serial
  • Descripción del producto
    Medical Device Safety Alert: Schiller Medical FRED easy & FRED easy Life Defibrillators
  • Manufacturer

Manufacturer