Alerta De Seguridad para Multiload Radiopaque Cu375 intrauterine contraceptive devices

Según Department of Health, este evento ( alerta de seguridad ) involucró a un dispositivo médico en Hong Kong que fue producido por Merck Sharp & Dohme (Asia) 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
    2013-03-27
  • 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
    Press release
  • Causa
    Recall of multiload radiopaque cu375 intrauterine contraceptive devices (with photos) the department of health (dh) today (march 26) instructed a local medical device supplier, merck sharp & dohme (asia) limited to recall one lot of multiload radiopaque cu375 intrauterine contraceptive devices (iucds), manufactured by an irish company, multilan ag, following discovery of impurities inside the packing of a number of devices. the discovery was made by dh's family health service (fhs) when they conducted routine inspection of stock prior to distributing the devices for use by their maternal and child health centres (mchcs). among some 300 iucds inspected belonging to lot number sm-3337-13, 4 devices were found to contain tiny hair-like or dust-like impurities inside their sterile pouches. so far, mchcs have not used iucds from the affected lot. the fhs reported the issue to the supplier as well as the medical device control office, which began investigation immediately. according to the supplier, about 950 devices from the affected lot were distributed to public and private hospitals and some private clinics. the dh has not received any relevant report of adverse incidents in hong kong. as a precautionary measure, the supplier is instructed to conduct a batch recall of the product with lot number sm-3337-13 from the market. the supplier has set up a hotline (3971 2913) for enquiries. healthcare professionals should stop using the affected products immediately. dh has brought the matter to relevant stakeholders' attention and will follow up on the investigation. ends.

Device

  • Modelo / Serial
  • Descripción del producto
    Press release: Recall of Multiload Radiopaque Cu375 intrauterine contraceptive devices (with photos)
  • Manufacturer

Manufacturer