Events

Alerte De Sécurité sur LifeVest 4000 Wearable Cardioverter Defibrillator

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

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
    2018-01-18
  • Date de publication de l'événement
    2018-01-18
  • 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_20180118.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.
  • Notes supplémentaires dans les données
    Medical Device Safety Alert
  • Cause
    Medical device safety alert: zoll lifevest 4000 wearable cardioverter defibrillator the food and drugs administration (fda), united states posted a medical device safety alert concerning lifevest 4000 wearable cardioverter defibrillator, manufactured by zoll. fda is providing information and recommendations regarding the zoll lifevest 4000 due to concerns that the device may fail to deliver treatment to the patient if the device is not replaced soon after displaying "call for service: device has a problem that may require service. call zoll for service, message code 102." ideally, the lifevest monitors the patient's heart, delivering a "treatment shock" as needed to restore the patient's heartbeat to a normal rhythm. however, fda is aware that in certain cases the lifevest 4000 may not be able to deliver a life-saving treatment shock to a patient due to a fault that prevents the device from charging its high-energy capacitors. during normal operation, this fault prompts the lifevest to display "call for service: device has a problem that may require service. call zoll for service, message code 102" on the device screen. the "message code 102" alert does not explicitly indicate to the patient that the device cannot be used and that the patient should call the manufacturer immediately. fda is aware of one patient death due to the lifevest's failure to deliver treatment as expected after message code 102 was displayed. according to the manufacturer, about 0.1% of the total devices distributed have displayed message code 102, which should only be remedied by immediate replacement of the device. the fda has provided recommendations for healthcare providers, patients and caregivers. for details, please visit the following fda website: https://www.Fda.Gov/safety/medwatch/safetyinformation/safetyalertsforhumanmedicalproducts/ucm592710.Htm https://www.Fda.Gov/medicaldevices/safety/alertsandnotices/ucm592583.Htm if you are in possession of the product, please contact your supplier for necessary actions. posted on 18 january 2018.

Device

LifeVest 4000 Wearable Cardioverter Defibrillator
  • Modèle / numéro de série
  • Description du dispositif
    Medical Device Safety Alert: Zoll LifeVest 4000 Wearable Cardioverter Defibrillator
  • Manufacturer
    Zoll

Manufacturer

Zoll