Events

Alerta De Seguridad para Plum A+ Infusion Volumetric Infusion Pump

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

¿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
    2014-03-14
  • Fecha de publicación del evento
    2014-03-14
  • País del evento
    Hong Kong
  • Fuente del evento
    DH
  • URL de la fuente del evento
    https://www.mdco.gov.hk/english/safety/recalls/recalls_20140314.html
  • 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.
    ICU Medical, Inc. acquired from Pfizer in early 2017, Hospira Infusion Systems, the portion of Hospira dedicated to develop infusion pumps.
  • Notas adicionales en la data
    Medical Device Safety Alert
  • Causa
    Medical device safety alert: plum a+ infusion volumetric infusion pump health canada has issued a medical device safety alert concerning plum a+ infusion volumetric infusion pump, manufactured by hospira. the authority has recently received a report that a hospira plum a+ pump was found to have an incorrectly positioned part resulting in a free flow of iv fluid when the door was opened. as a result of this recent incident, healthcare professionals are reminded to ensure that tubing is clamped when the door of an infusion pump is opened to avoid a potential risk of unrestricted gravity flow. patients using these devices in a home setting should not stop using their infusion pump unless advised to do so by their healthcare provider. for details, please refer to the health canada website:http://www.Healthycanadians.Gc.Ca/recall-alert-rappel-avis/hc-sc/2014/38391a-eng.Php if you are in possession of the affected product, please contact your supplier for necessary actions. posted on 14 march 2014.

Device

Plum A+ Infusion Volumetric Infusion Pump
  • Modelo / Serial
  • Descripción del producto
    Medical Device Safety Alert: Plum A+ Infusion Volumetric Infusion Pump
  • Manufacturer
    Hospira

Manufacturer

Hospira
  • Empresa matriz del fabricante (2017)
    Pfizer
  • Source
    DH