AutoSPECT Pro Reconstruction application on Extended Brilliance Workplace NM software version 2.0(used to process, analyse, and display medical images/data obtained from other diagnostic devices, including gamma cameras) 의 리콜

Department of Health, Therapeutic Goods Administration에 따르면, 해당 리콜 는 Australia 에서 Philips Electronics Australia 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-00384-1
  • 사례 위험등급
    Class II
  • 사례 시작날짜
    2016-04-06
  • 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
    The autospect pro application was only designed to reconstruct cardiac spect data obtained with detectors positioned at 90° or 180° relative to one another. however, certain gamma cameras, e.G., the marconi axis and irix cameras, permit acquisitions at other relative detector angles. data acquired at these other angles will not be correctly reconstructed by autospect pro, and the results will likely be erroneous.Incorrect computational results may lead, under certain circumstances to misdiagnosis, e.G., an incorrect assessment of a patient’s myocardial perfusion, in which case, the patient may not receive further indicated diagnostic tests or therapy, putting the patient at risk of a subsequent cardiovascular event.Philips has not received any report of any patient harm associated with this issue.
  • 조치
    Philips is advising users to follow instructions in the customer letter to determine whether the system is affected. If it is affected, users are asked NOT to use the AutoSPECT Pro application on the affected data sets until Philips modifies its software to prevent it from reconstructing data acquired using these modes. Instead, use the reconstruction applications on the camera’s native processing computers (e.g. Odyssey). Philips is recommending a review of previously processed data based on the clinical context. This action has been closed-out on 27/01/2017.

Device

  • 모델명 / 제조번호(시리얼번호)
    AutoSPECT Pro Reconstruction application on Extended Brilliance Workplace NM software version 2.0(used to process, analyse, and display medical images/data obtained from other diagnostic devices, including gamma cameras)ARTG Number: 117441
  • Manufacturer

Manufacturer

  • 제조사 모회사 (2017)
  • Source
    DHTGA