Merge PACS (Amicas PACS) with software versions 6.0.2.0 MR2, 6.0.3.0 MR3, 6.0.3.1 MR3 CU1 (used for medical imaging acquisition) 의 리콜

Department of Health, Therapeutic Goods Administration에 따르면, 해당 리콜 는 Australia 에서 Emergo Asia Pacific Pty Ltd T/a Emergo Australia 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-00861-1
  • 사례 위험등급
    Class II
  • 사례 시작날짜
    2016-06-29
  • 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
    This action has been initiated due to potential incorrect display of mammographic measurements. the problem is that there is variability of how the estimated radiographic magnification factor (ermf) is provided in the dicom header data. when measuring a lesion on an unmagnified mammography image then performing the same measurement on an image magnified by the hologic imager (different image) the measurements are not the same. use of this product may lead to additional imagining, such as mri and/or biopsy follow-up, before referring a patient to any surgical procedures. particularly if an mri or ultrasound is done the incorrect measurements would be identified as erroneous. this may result in a delay in diagnosis or treatment or patient misdiagnosis.
  • 조치
    A software upgrade will be implemented as a permanent correction. In the interim, users are advised not to use Merge PACS mammographic measurements until upgraded. The ability to create any measurements and annotations are controlled by together by a set of privileges which should be disabled until upgraded. This action has been closed-out on 22/02/2017.

Device

  • 모델명 / 제조번호(시리얼번호)
    Merge PACS (Amicas PACS) with software versions 6.0.2.0 MR2, 6.0.3.0 MR3, 6.0.3.1 MR3 CU1 (used for medical imaging acquisition)ARTG Number: 191068
  • Manufacturer

Manufacturer