Alerta De Seguridad para Defibrillation electrodes

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

¿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
    2016-02-11
  • Fecha de publicación del evento
    2016-02-11
  • 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: leonhard lang defibrillation electrodes medical device manufacturer, leonhard lang, has issued a medical device safety alert concerning its defibrillation electrodes. the affected models are: 50017 – skintact (df30l), 50018 – skintact (df32l), mindray mr-61 (df39g), 50611 – mindray mr-61 (df74gc), 50617 – cariaid (df73gc), 50626 – weinmann pediatric (df71g), 50636 – osatu pediatric ksa 0501 b (df75g), 50645 – skintact (df72g), 59945 – skintact (df31l) and 59966 – skintact (df35l). in the course of in-house shelf-life tests, performed in addition to accelerated aging tests, the manufacturer has identified the potential risk of sparkover, which may result in a malfunction of these defibrillation electrodes. the potential malfunction can occur with these electrodes after a duration of storage of about 28 months or more. all electrodes with a duration of storage of 28 months or less show a faultless performance and can be used as usual according to the instructions for use. according to the manufacturer, there is a risk that the affected electrodes will exhibit this malfunction before reaching the indicated expiration date. this may cause a situation in which a patient, who is in a life-threatening condition and requires a defibrillation shock, cannot be treated in good time. the precise cause for this is still under investigation. the manufacturer requests users to immediately stop using and destroy the affected products. product recall is on-going. if you are in possession of the affected products, please contact your supplier for necessary actions. posted on 11 february 2016.

Device

  • Modelo / Serial
  • Descripción del producto
    Medical Device Safety Alert: Leonhard Lang Defibrillation electrodes
  • Manufacturer

Manufacturer