Fujifilm Digital Mammography System 의 리콜

Department of Health, Therapeutic Goods Administration에 따르면, 해당 리콜 는 Australia 에서 Fujifilm 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-2017-RN-00903-1
  • 사례 위험등급
    Class II
  • 사례 시작날짜
    2017-07-25
  • 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
    Fujifilm has identified that in very rare cases, software versions v5.0, v5.1, v5.2, v6.0, v6.1 and v7.00 for specific workstations within the digital mammography system may possibly assign a duplicated id number to exposure images.Transmitting the image with the duplicated id number assigned to a pacs could possibly overwrite the image in an old study stored on the pacs. this would cause an unexpected image to appear when referring to the old study. the image and data of a new study does not have this issue, therefore, there is no effect on a diagnosis.Fujifilm has corrected the software that is the cause of such failure.
  • 조치
    FUJIFILM has corrected the software that is the cause of such failure. Actions to be taken by customer/user: Make sure the latest images transmitted to PACS exists in the new study-where it should be. If the image with the duplicated ID number assigned is transmitted to PACS, you will fail to find it in a newly created study. (ie it is missing). This is because the image transmitted to PACS with that error overwrites an existing(older) study image and is stored in another(older) study. If you have this error, please contact your local FUJIFILM office. Although the probability of the above error is very rare, systematically checking that the correct number of images per patient has been transferred to the PACS will make sure in case such errors occur.

Device

  • 모델명 / 제조번호(시리얼번호)
    Fujifilm Digital Mammography SystemWorkstations:Amulet (FDR MS-1000)Amulet (FDR MS-2500)Amulet Innovality (FDR MS-3500)CR-IR363AWSSoftware versions: v5.0, v5.1, v5.2, v6.0, v6.1 and v7.0 ARTG Number:159785
  • Manufacturer

Manufacturer