BrainLab Navigation Software Spine and Trauma 3D 2.0 (intra-operative image guided stereotactic localisation system to enable precision spine and trauma surgeries) 의 리콜

Department of Health, Therapeutic Goods Administration에 따르면, 해당 리콜 는 Australia 에서 Brainlab 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-2013-RN-01266-1
  • 사례 위험등급
    Class I
  • 사례 시작날짜
    2013-11-28
  • 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
    In the ‘fluoro match registration’ function when used in combination with a digitally integrated c-arm, the software algorithm may not find an adequate match between the intraoperatively acquired 2d fluoroscopic images and the preoperative ct or other compatible 3d datasets. due to a software anomaly the intraoperative 2d fluoroscopic images are not correctly processed, causing a low contrast of the images potentially resulting in the software algorithm being unable to find a correct match between the low contrast 2d fluoroscopic images and the segmented area of the 3d dataset. alternatively, it may incorrectly match the segmented area to the spine reference x-clamp. for an incorrect match, the display of instruments by the navigation system would be shifted compared to the actual patient anatomy. if this is not detected during user verification, deviation of position information could impact clinical decisions which could lead to ineffective treatment, serious injury or patient death.
  • 조치
    Brainlab will provide a software update to affected customers with this issue resolved. As a temporary solution, until the software update has been implemented, users of the Navigation Software Spine & Trauma 3D 2.0 are advised to adhere to the workaround instructions in the customer letter. This action has been closed-out on 01/02/2016.

Device

  • 모델명 / 제조번호(시리얼번호)
    BrainLab Navigation Software Spine and Trauma 3D 2.0 (intra-operative image guided stereotactic localisation system to enable precision spine and trauma surgeries)ARTG Number: 96517
  • Manufacturer

Manufacturer