Events

Alerte De Sécurité sur Medi-Trace Cadence Adult Multi-Function Defibrillation Electrodes

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

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
    2015-09-02
  • Date de publication de l'événement
    2015-09-02
  • 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_20150902.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: covidien medi-trace cadence adult multi-function defibrillation electrodes the therapeutic goods administration (tga) of australia has posted a medical device safety alert concerning medi-trace cadence adult multi-function defibrillation electrodes (pre-connect), manufactured by covidien. the affected item numbers are 22550pc and 22770pc, with lot numbers 517521x, 519835x, 516313x, 519124x and 513426x. according to the alert, a recall was being conducted due to a low-level potential for damage to the wire insulation which was identified during a review of the manufacturing process. the use of products with this condition may result in a potentially increased risk for reduced or no patient therapy, arcing of current, sparking, and patient and/or clinician burns. according to the safety alert, no patient injuries have been reported related to this damaged wire insulation issues. users are advised to immediately quarantine and discontinue use of the affected devices. for details, please refer to the tga website:http://apps.Tga.Gov.Au/prod/sara/arn-detail.Aspx?k=rc-2015-rn-00803-1 if you are in possession of the affected products, please contact your supplier for necessary actions. posted on 2 september 2015.

Device

Medi-Trace Cadence Adult Multi-Function Defibrillation Electrodes
  • Modèle / numéro de série
  • Description du dispositif
    Medical Device Safety Alert: Covidien Medi-Trace Cadence Adult Multi-Function Defibrillation Electrodes
  • Manufacturer
    Covidien

Manufacturer

Covidien
  • Société-mère du fabricant (2017)
    Medtronic plc
  • Commentaire du fabricant
    “If our surveillance systems identify a potential performance issue, our personnel promptly evaluate the problem, including, when appropriate, conducting root cause investigations and internal testing to assess whether the product continues to meet specifications and defined performance criteria,” Medtronic told ICIJ in a statement. “In some cases, based on this evaluation, Medtronic may determine that a recall is necessary.” The company said that it communicates with healthcare providers and/or patients and provide recommendations to address such issues. Medtronic noted that these communications can include letters, emails, calls, press releases, physician notifications and social media postings, as well as informing the FDA and other regulators of the actions.
  • Source
    DH