Rappel de ACUSON SC2000 System (Ultrasound cardiovascular imaging system) when used with V5M Transducer (which includes revision 4 of the MPI board)

Selon Department of Health, Therapeutic Goods Administration, ce/cet/cette rappel concerne un dispositif en/au/aux/à Australia qui a été fabriqué par Siemens 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-00325-1
  • Classe de risque de l'événement
    Class II
  • Date de mise en oeuvre de l'événement
    2013-04-24
  • Pays de l'événement
  • Source de l'événement
    DHTGA
  • 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
    When using the v5m transducer, the display of the temperature on the acuson sc2000 system can be lower than the actual temperature of the v5m transducer. this occurs only if the system hardware contains revision 4 of the mpi board. if this condition occurs when scanning a febrile or hyperthermic patient using maximum system power settings (0 db), the actual lens surface temperature could exceed 43degc while the system temperature display continues to show a value under 43degc. there is a potential to cause oesophageal burns in patients with body temperatures greater than 40degc.Products supplied in australia include a different transducer (4z1c) which cannot be used for trans-oesophageal imaging. potential for heating with this model is mitigated by independent mechanical cooling which is not dependent on a feedback mechanism. siemens is correcting all models including revision 4 of the mpi board irrespective of the transducer version.
  • Action
    Siemens is providing temporary work around instructions and is implementing an upgrade of the system hardware that will correct the issue.

Device

  • Modèle / numéro de série
    ACUSON SC2000 System (Ultrasound cardiovascular imaging system) when used with V5M Transducer (which includes revision 4 of the MPI board)ARTG Number: 139591
  • Manufacturer

Manufacturer

  • Société-mère du fabricant (2017)
  • Source
    DHTGA