Alerta De Seguridad para ClearSight Heart Reference Sensor

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

¿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
    2017-12-14
  • Fecha de publicación del evento
    2017-12-14
  • 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: edwards lifesciences clearsight heart reference sensor medical device manufacturer, edwards lifesciences, has issued a medical device safety alert concerning its clearsight heart reference sensor [model number: evhrs; all serial numbers manufactured after 31 december 2015]. the current product as well as the affiliated labeling contains an expiration date of two years. through investigation and analysis of complaint data, the manufacturer discovered that hrs units are susceptible to experiencing an “hrs out of range” error message in the ev1000 platform that is beyond six months from the date of manufacture. as a result, the manufacturer has decided to change the expiration date to six months from the date of manufacture. additionally, this change will also require replacing the operator’s manual of the ev1000 clinical platform and the instructions for use (ifu) of the heart reference sensor. according to the manufacturer, this issue poses no risk to patients as the ev1000 clinical platform will not allow the clinician to zero the device and initiate monitoring. this would create a pre-procedural delay while the troubleshooting process is completed. affected users could continue to use the product. if the user does not encounter the “hrs out of range” message on the ev1000 clinical platform, the heart reference sensor is functioning properly and can be safely used to monitor your patients. if the user encounters the “hrs out of range” message on the ev1000 clinical platform, he/she should contact the manufacturer’s technical support. product replacement is on-going. according to the local supplier, the affected products are not distributed in hong kong. if you are in possession of the affected products, please contact your supplier for necessary actions. posted on 14 december 2017.

Device

  • Modelo / Serial
  • Descripción del producto
    Medical Device Safety Alert: Edwards LifeSciences ClearSight Heart Reference Sensor
  • Manufacturer

Manufacturer