Alerta De Seguridad para Vital Signs Hygroscopic Condenser Humidifier Passive Humidification Device (HCH) for Vital Signs Anesthesia Breathing Circuits

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

¿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
    2011-08-04
  • 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
    Fda class i recall: ge healthcare vital signs hygroscopic condenser humidifier passive humidification device (hch) for vital signs anesthesia breathing circuits it has come to our attention that the u.S. food and drug administration (fda) has issued a class i recall concerning ge healthcare vital signs hygroscopic condenser humidifier passive humidification device (hch) for vital signs anesthesia breathing circuits. the vital signs hch is sold as part of the vital signs anesthesia breathing circuit. an hch is used to maintain moisture in the patient's airway during mechanical ventilation. the affected device may have an occlusion that can prevent proper flow of the medical gases or oxygen, possibly resulting in insufficient oxygen delivered to the patient. clinical users have been directed to not use the anesthesia circuits containing the vital signs devices passive humidification device (hygroscopic condenser humidifier, or "hch"), or the stand alone hch device with the affected product item numbers and lot numbers, and to isolate all affected product. according to the local supplier, hong kong is not affected. for details, please visit the following fda website: http://www.Fda.Gov/medicaldevices/safety/listofrecalls/ucm266542.Htm if you are in possession of the affected product, please contact your supplier for necessary actions.

Device

  • Modelo / Serial
  • Clasificación del producto
  • Descripción del producto
    Medical Device Safety Alert: [4 Aug 2011] GE Healthcare Vital Signs Hygroscopic Condenser Humidifier Passive Humidification Device (HCH) for Vital Signs Anesthesia Breathing Circuits
  • Manufacturer

Manufacturer