Alerta De Seguridad para VIDAS D-Dimer Exclusion II

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

¿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
    2013-04-16
  • Fecha de publicación del evento
    2013-04-16
  • 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: biomerieux vidas d-dimer exclusion ii medical device manufacturer, biomerieux, has issued a field safety notice concerning the vidas d-dimer exclusion ii [reference no.: 30455 and 30455-01]. the manufacturer has registered some customer complaints about not reproducible results below the detection limit (<45 ng/ml) on the above listed lot numbers. the manufacturer’s internal investigation after testing in-house titrated samples has not reproduced this result. the potential risk associated to this issue is reporting false negative results for vidas d-dimer exclusion ii. the impact of a false negative d-dimer test result could be critical for the patient with a low or moderate clinical pretest probability for deep vein thrombosis (dvt) or pulmonary embolism (pe) because it could prevent further diagnostic workup for venous thromboembolism and withholding anticoagulant treatment when it is actually needed, resulting in a negative impact to patient care. the manufacturer advises all affected users to take the following actions:- repeat all results less than < 45 ng/ml obtained with the kit vidas® d-dimer exclusion ii™ ref. 30455 and 30455-01. determine if retrospective analysis of results of the patients is required and investigate further (e.G. final diagnosis and clinical status of the patient) if the result is < 45 ng/ml. an additional insert will be added to newly manufactured lots to require a confirmation of the results below the detection limit (< 45 ng/ml). according to the local supplier, the affected devices were distributed in hong kong. if you are in possession of the affected products, please contact your supplier for necessary actions. posted on 16 april 2013.

Device

  • Modelo / Serial
  • Descripción del producto
    Medical Device Safety Alert: Biomerieux VIDAS D-Dimer Exclusion II
  • Manufacturer

Manufacturer