Alerta De Seguridad para Salmonella paratyphi A-H Stained Suspension

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

¿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
    2018-05-23
  • Fecha de publicación del evento
    2018-05-23
  • 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: thermo scientific remel salmonella paratyphi a-h stained suspension medical device manufacturer, remel europe limited (part of thermo fisher scientific), has issued a medical device safety alert concerning its thermo scientific remel salmonella paratyphi a-h stained suspension. the affected products are identified as below: product code: r30855101 bottle lot number: 2169556 carton lot number: 2184561, 2308897, 2228271, 2213610 & 2258333 according to the manufacturer, an internal technical investigation has determined that the salmonella paratyphi a-h stained suspension (r30855101) is showing granularity, upon dispensing, which may be misinterpreted as a positive result when used according to the instructions for use (ifu). the clinical risk is extremely low based on the following rationale: the serological test method is performed primarily for epidemiological purposes, and will not have any direct clinical effect critical to patient care. the tests should be used in parallel with appropriate culture techniques for the isolation and identification of the causative organism; any risk to patients is indirect, in that epidemiology in a population may not be profiled accurately. the affected users are advised to take the following actions: review any remaining inventory of salmonella paratyphi a-h stained suspension (r30855101); requirement for review of reported test results should be determined by the appropriate technical expert. according to the local supplier, the affected products are distributed in hong kong. if you are in possession of the affected products, please contact your supplier for necessary actions. posted on 23 may 2018.

Device

  • Modelo / Serial
  • Descripción del producto
    Medical Device Safety Alert: Thermo Scientific Remel Salmonella paratyphi A-H Stained Suspension
  • Manufacturer

Manufacturer