FUJIFILM FDR-1000AWS / FDR-2000AWS / FDR-3000AWS V5.1.0001-0007 with Biopsy unit (a component of 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-2014-RN-00479-1
  • 사례 위험등급
    Class II
  • 사례 시작날짜
    2014-04-24
  • 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
    It was found that for software v5.1.0001-0007 used in workstation (aws), which is a component of fujifilm digital mammography system, when image enhancement processing is performed on the exposed image with an option function during biopsy, the screen may not return to the original image. depending on the enhancement parameter, the calcification may seem unclear compared to the original image. therefore, there is a potential that the tip of needle cannot reach the desired biopsy area. furthermore, after collecting the target sample, it may be difficult to ascertain whether the necessary calcification part has been properly extracted. due to these reasons, the occurrence of this issue may precipitate that a re-examination might be necessary. this image processing is an option for biopsy and does not affect other normal exposures.
  • 조치
    Customers are advised to not perform image enhancement during Biopsy. In the case that a calcification becomes unclear due to enhancement processing, select the weakest enhancement processing or redisplay the image on the 1st monitor by right-clicking. FUJIFILM service personnel will contact the affected facility to arrange for a software update as a corrective measure.

Device

  • 모델명 / 제조번호(시리얼번호)
    FUJIFILM FDR-1000AWS / FDR-2000AWS / FDR-3000AWS V5.1.0001-0007 with Biopsy unit (a component of FUJIFILM Digital Mammography System)Serial Number: 37020038ARTG Number: 159785
  • Manufacturer

Manufacturer