Events

Rappel de Single and dual LCD monitor suspensions used on Precision RXi fluoroscopic imaging systems

Selon Department of Health, Therapeutic Goods Administration, ce/cet/cette rappel concerne un dispositif en/au/aux/à Australia qui a été fabriqué par GE Healthcare Australia 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
    Recall
  • ID de l'événement
    RC-2015-RN-00575-1
  • Classe de risque de l'événement
    Class II
  • Date de mise en oeuvre de l'événement
    2015-06-26
  • 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-2015-RN-00575-1
  • 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
    Ge healthcare has become aware of a reported incident where a monitor fell from the suspension. a fall of a monitor could result in an injury to a patient or operator. there have been no injuries reported as a result of this issue.
  • Action
    A GE Healthcare representative will contact affected customers to arrange for the correction. In the interim, users are advised to perform a visual check before and after each use for the presence of the four (4) mounting screws. Check the secureness of these screws by hand. If these screws are present and secure, users may continue use of the system. If any of these screws are missing or can easily be turned by hand, follow the precautions below before continuing use with the monitor(s). - Position the monitor suspension in the most frequently used position and limit further movement as much as possible. - Clearly inform (e.g. through signage and verbal instructions) the users and other auxiliary personnel who may come in contact with the system to not move the monitor suspension once in position. - Contact the GE Healthcare representative to inform them of any loose or missing screws. This action has been closed-out on 17/08/2016.

Device

Single and dual LCD monitor suspensions used on Precision RXi fluoroscopic imaging systems
  • Modèle / numéro de série
    Single and dual LCD monitor suspensions used on Precision RXi fluoroscopic imaging systemsARTG Number: 99423
  • Manufacturer
    GE Healthcare Australia Pty Ltd

Manufacturer

GE Healthcare Australia Pty Ltd