MAGiC (MAGnetic resonance image Compilation) on Signa Pioneer MRI systems running application software version DV25.1 의 리콜

Department of Health, Therapeutic Goods Administration에 따르면, 해당 리콜 는 Australia 에서 GE Healthcare Australia Pty Ltd 에 의해 제조된 제품과 관련되어 있습니다.

이것은 무엇인가요?

의료기기에 문제가 생겼을 경우 제조사가 이를 바로잡거나 시장에서 회수하는 조치를 말한다. 회수(Recall)는 의료기기에 결함이 있거나, 건강에 위협이 되거나, 또는 결함도 있고 건강에도 위협이 될 경우에 발생한다.

데이터에 대해 더 자세히 알아보기 여기
  • 사례 유형
    Recall
  • 사례 ID
    RC-2016-RN-01213-1
  • 사례 위험등급
    Class II
  • 사례 시작날짜
    2016-09-19
  • 사례 국가
  • 사례 출처
    DHTGA
  • 사례 출처 URL
  • 비고 / 경고
    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.
  • 데이터 추가 비고
  • 원인
    Ge healthcare has recently become aware of a potential safety issue with the magic imaging application. images may exhibit novel artefacts on magic t2 flair synthetic reconstructions that may be difficult to recognise without access to conventional t2 flair weighted images. this issue has the potential to lead to misinterpretation of the magic images when making medical diagnosis or treatment decisions. with magic acquisition all contrasts are acquired simultaneously, therefore any gross patient motion will impact all generated images and may further alter the presentation of the aforementioned novel artefacts. there have been no injuries reported as a result of this issue.
  • 조치
    GE will be correcting all affected products and providing MAGiC operator documentation Release Notes. In the interim, GE is advising users that they may continue to use MAGiC with the following precautions: Exercise caution when reviewing CSF spaces, its adjacent tissues and the posterior fossa, particularly for cases involving subtle pathology. If in doubt, it is advisable to acquire a conventional 2D or 3D T2 FLAIR series or a MAGIC series in a different orientation for cross-sequence comparison. It is always recommended to pay close attention to patient stabilisation during scanning. Attention should be given to prior cases as they may be affected by this safety issue. For historical data inquiries, contact GE service for assistance in identifying any affected images. This action has been closed out on 15 June 2017.

Device

  • 모델명 / 제조번호(시리얼번호)
    MAGiC (MAGnetic resonance image Compilation) on Signa Pioneer MRI systems running application software version DV25.1 ARTG Number: 252692
  • Manufacturer

Manufacturer