Events

Rappel de Brilliance CT 64, Ingenuity Core, Ingenuity Core 128 systems using software versions 2.6.1 or 3.5.4 (Computed tomography full-body x-ray system)

Selon Department of Health, Therapeutic Goods Administration, ce/cet/cette rappel concerne un dispositif en/au/aux/à Australia qui a été fabriqué par Philips Electronics Australia 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
    Recall
  • ID de l'événement
    RC-2013-RN-00423-1
  • Classe de risque de l'événement
    Class II
  • Date de mise en oeuvre de l'événement
    2013-05-09
  • Pays de l'événement
    Australia
  • Source de l'événement
    DHTGA
  • URL de la source de l'événement
    https://apps.tga.gov.au/Prod/sara/arn-detail.aspx?k=RC-2013-RN-00423-1
  • 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
    Philips healthcare received reports that certain brilliance ct 64 ingenuity core systems running software versions 2.6.1 or 3.5.4 exhibited intermittent swirl-like ring artifacts that may appear on reconstructed images, which may impair the diagnostic quality of affected images.
  • Action
    Philips Healthcare is advising that clinical judgment should be used by the customer/user to determine if the images contained in the dataset without artifacts contain enough information to make a diagnosis. If these images are sufficient, no further action is required. If the images are not sufficient, a re-scan of the patient is required. Philips Healthcare is implementing software update versions 2.6.2 or 3.5.5 to permanently correct the issue. This action has been closed-out on 12/02/2016.

Device

Brilliance CT 64, Ingenuity Core, Ingenuity Core 128 systems using software versions 2.6.1 or 3.5...
  • Modèle / numéro de série
    Brilliance CT 64, Ingenuity Core, Ingenuity Core 128 systems using software versions 2.6.1 or 3.5.4 (Computed tomography full-body x-ray system)ARTG Number: 98868
  • Manufacturer
    Philips Electronics Australia Ltd

Manufacturer

Philips Electronics Australia Ltd
  • Société-mère du fabricant (2017)
    Philips
  • Source
    DHTGA