Alerte De Sécurité sur Life Pulse High-Frequency Ventilator Patient Circuits

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

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
    2012-12-06
  • Date de publication de l'événement
    2012-12-06
  • Pays de l'événement
  • Source de l'événement
    DH
  • URL de la source de l'événement
  • 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.
  • Notes supplémentaires dans les données
    Medical Device Safety Alert
  • Cause
    Medical device safety alert: bunnell life pulse high-frequency ventilator patient circuits the united states food and drug administration (fda) posted a firm press release concerning life pulse high-frequency ventilator patient circuits, manufactured by bunnell incorporated. bunnell incorporated voluntarily initiated a nationwide recall notification of life pulse high-frequency ventilator patient circuits. the product has been found to have heater wire insulation that can melt, causing sparking and smoke close to the humidifier cartridge. there have been 12 reported failures out of 5,771 patient circuits distributed. although there have been no reports of patient injury or death the manufacturer informs clinicians to be aware of the potential that a patient circuit failure could result in patient injury or death as a precautionary measure. for details, please refer to the following fda website: http://www.Fda.Gov/safety/recalls/ucm330842.Htm. if you are in possession of the affected product, please contact your supplier for necessary actions. posted on 6 december 2012.

Device

  • Modèle / numéro de série
  • Classification du dispositif
  • Description du dispositif
    Medical Device Safety Alert: Bunnell Life Pulse High-Frequency Ventilator Patient Circuits
  • Manufacturer

Manufacturer