Alerta De Seguridad para Dual Hemo MCable pod used with the Infinity Acute Care System (IACS) Monitoring Solution

Según Department of Health, este evento ( alerta de seguridad ) involucró a un dispositivo médico en Hong Kong que fue producido por Dräger Medical 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
    2017-10-03
  • Fecha de publicación del evento
    2017-10-03
  • 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
    Field safety notice: dräger dual hemo mcable pod used with the infinity acute care system (iacs) monitoring solution medical device manufacturer, dräger medical systems, inc., has issued a safety alert concerning its dual hemo mcable pod used with the infinity acute care system (iacs) monitoring solution. the manufacturer has determined through internal testing that dual hemo mcable pods with revision index (ri) 15 and 16, which are used with the dräger infinity acute care system, may permit liquid ingress inconsistent with their ipx4 rating, which could potentially result in an incorrect measured value of invasive blood pressure. the manufacturer has not received any complaints and is not aware of any negative patient consequences arising from this issue. revisions prior to ri 15, with proper orientation will still maintain its designated ipx1 rating and are not within the scope of this safety notice. in addition, revisions labelled ri 17 and greater are not affected by this notice because these revisions continue to meet the ipx4 standard. affected users are requested to take the following actions: contact the manufacturer to receive a sleeve that can be applied to protect against liquid ingress see the safety notice provided by the manufacturer for required upright orientation of the dual hemo mcable pod and installation instructions for the sleeve. according to the local supplier, the affected product is distributed in hong kong. if you are in possession of the affected products, please contact your supplier for necessary actions. posted on 3 october 2017.

Device

  • Modelo / Serial
  • Descripción del producto
    Medical Device Safety Alert: Dräger Dual Hemo MCable pod used with the Infinity Acute Care System (IACS) Monitoring Solution
  • Manufacturer

Manufacturer