Events

Alerte De Sécurité sur Plum A+ Infusion Volumetric Infusion Pump

Selon Department of Health, ce/cet/cette alerte de sécurité concerne un dispositif en/au/aux/à Hong Kong qui a été fabriqué par Hospira.

Qu'est-ce que c'est?

Les alertes fournissent des informations importantes et des recommandations concernant les dispositifs médicaux. Le fait qu'une alerte soit émise ne signifie pas nécessairement qu'un dispositif soit dangereux. Les alertes de sécurité, qui sont envoyées tant aux travailleurs du secteur médical qu'aux utilisateurs de ces dispositifs, peuvent inclure des rappels. Elles peuvent être rédigées par des fabricants mais aussi par des autorités en charge de la santé.

En savoir plus sur les données ici
  • Type d'événement
    Safety alert
  • Date
    2014-03-14
  • Date de publication de l'événement
    2014-03-14
  • Pays de l'événement
    Hong Kong
  • Source de l'événement
    DH
  • URL de la source de l'événement
    https://www.mdco.gov.hk/english/safety/recalls/recalls_20140314.html
  • Notes / Alertes
    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.
  • Notes supplémentaires dans les données
    Medical Device Safety Alert
  • Cause
    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
  • Modèle / numéro de série
  • Description du dispositif
    Medical Device Safety Alert: Plum A+ Infusion Volumetric Infusion Pump
  • Manufacturer
    Hospira

Manufacturer

Hospira
  • Société-mère du fabricant (2017)
    Pfizer
  • Source
    DH