Rappel de Medtronic Xomed Instrument Trays

Selon Department of Health, Therapeutic Goods Administration, ce/cet/cette rappel concerne un dispositif en/au/aux/à Australia qui a été fabriqué par Medtronic Australasia Pty Ltd.

Qu'est-ce que c'est?

Une correction ou un retrait opéré par un fabricant afin de répondre à un problème causé par un dispositif médical. Les rappels surviennent lorsqu'un dispositif médical est défectueux, lorsqu'il pourrait poser un risque pour la santé, ou les deux à la fois.

En savoir plus sur les données ici
  • Type d'événement
  • ID de l'événement
  • Classe de risque de l'événement
    Class II
  • Date de mise en oeuvre de l'événement
  • Pays de l'événement
  • Source de l'événement
  • URL de la source de l'événement
  • Notes / Alertes
    Australian data is current through July 2018. All of the data comes from the Australian Therapeutic Goods Administration, 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 recall data from the U.S. and Australia.
  • Notes supplémentaires dans les données
  • Cause
    During the validation of a new instrument, testing revealed that use of a gravity steam cycle with one of the listed instrument trays did not produce the sterility assurance level (sal) of 10-6 required by industry standard (ansi/aami st77:2006). a subsequent investigation of all medtronic xomed instrument trays identified additional trays as having certain locations within the tray that would not meet the recommended sterilization level of sal 10-6 during gravity steam sterilization cycles.
  • Action
    Hospitals that use GRAVITY steam sterilisation cycles are requested to quarantine all stock immediately. Hospitals that use PREVACUUM steam sterilisation are advised that they can continue to use the trays once they have attached a label stating 'PREVACUUM ONLY' provided by Medtronic. A Medtronic representative will be in contact with customers to arrange for replacement with a new tray with updated labelling.


  • Modèle / numéro de série
    Medtronic Xomed Instrument Trays Lot Numbers: All lots distributed prior to July 2013Multiple Product Numbers
  • Manufacturer


  • Société-mère du fabricant (2017)
  • 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