Alerta De Seguridad para EXACTAMIX Compounder EM2400 and EM1200

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

¿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
    2013-08-27
  • Fecha de publicación del evento
    2013-08-27
  • 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: baxter healthcare exactamix compounder em2400 and em1200 medical device manufacturer, baxter healthcare ltd, has issued a medical device safety alert concerning the exactamix compounder em2400 and em1200, display module 2400- dy and 1200-dy. baxter has received customer complaints regarding exactamix compounders experiencing an intermittent reset of the internal clock contained within the exactamix compounder display module with part numbers 2400-dy and 1200-dy. this issue only affects the dy display modules. this condition is the result of the battery life being less than anticipated and impacting the internal clock of the compounder. this battery failure results in failure of the exactamix system to alert the user to replace the disposable set after 24 hours of use. users should not rely on this alert to trigger the daily replacement of disposable sets. because daily replacement of disposable sets is standard practice, no adverse health consequence is reasonably expected to result. potential hazards which could result if the disposable sets are not replaced daily include microbial contamination and particulate matter. there have been no reported patient injuries or adverse events associated with this issue. the manufacturer reminds users that confirming the correct time and date is a best practice, and should be performed at the setup of each use. the manufacturer also recommends users to create and review the authorization report daily, which will allow users to confirm their compounder has the correct time and date. in addition, the manufacturer will arrange a swap-out of the current display model with a unit that has had a correction applied. according to the local supplier, the affected products were distributed in hong kong. if you are in possession of the affected products, please contact your supplier for necessary actions. posted on 27 august 2013.

Device

  • Modelo / Serial
  • Descripción del producto
    Medical Device Safety Alert: Baxter Healthcare EXACTAMIX Compounder EM2400 and EM1200
  • Manufacturer

Manufacturer