Alerta De Seguridad para BURETROL Solution Set with 150ml INTERLINK Burette

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

¿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
    2014-07-25
  • Fecha de publicación del evento
    2014-07-25
  • 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: baxter buretrol solution set with 150ml interlink burette medical device manufacturer, baxter healthcare, has issued a field safety notice (fsn) concerning its buretrol solution set with 150ml interlink burette. the affected product code is 2c7564 with the lot numbers dr13e06019, dr13j24021, dr13j24039 and dr13l11016. the affected products were distributed to customers between 14 march 2014 and 30 june 2014. according to the manufacturer, the voluntary recall was issued due to complaints of separation between the burette chamber and the drip chamber. the root cause for this issue has been identified and resolved. if the separation is not detected before connection with the administration set, there is a risk of contamination of the sterile fluid path which could lead to blood stream infection or sepsis and may be life-threatening. additionally, air may be aspirated into the vascular system, causing venous air embolism, which while is improbable may be life-threatening. there have been no adverse events reported for this issue. 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 25 july 2014.

Device

  • Modelo / Serial
  • Descripción del producto
    Medical Device Safety Alert: Baxter BURETROL Solution Set with 150ml INTERLINK Burette
  • Manufacturer

Manufacturer