Alerta De Seguridad para Mass Spectrometry Instruments

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

¿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
    2012-10-24
  • Fecha de publicación del evento
    2012-10-24
  • 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: waters corporation mass spectrometry instruments medical device manufacturer, waters corporation, has initiated a medical device field safety corrective action concerning various models of mass spectrometry instruments. the affected models can be identified as follows:- waters acquity tqd; acquity sqd; lct premier xe; quattro premier; quattro premier xe; quattro micro; xevo g2 tof; xevo tq; xevo tqd & zq 2000 the manufacturer initiated this voluntary medical device correction because there is a possibility that the ion block source heater may fail. in some instances, the failure could cause a short term loss of or variation in sensitivity that may subsequently lead to inaccurate data. the loss of or variation in sensitivity is most pronounced in assays with shorter dwell times (i.E. less than 100 ms) and may not always be detected by quality control and internal standard value monitoring. no adverse events have been reported as a result of this potential issue. according to the manufacturer, the affected devices were distributed in hong kong. if you are in possession of the affected product, please contact your supplier for necessary actions. posted on 24 october 2012.

Device

  • Modelo / Serial
  • Descripción del producto
    Medical Device Safety Alert: Waters Corporation Mass Spectrometry Instruments
  • Manufacturer

Manufacturer