DRX Revolution Mobile, DRX Mobile Retrofit & DRX Transportable X-ray Systems 의 리콜

Department of Health, Therapeutic Goods Administration에 따르면, 해당 리콜 는 Australia 에서 Carestream Health 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-00970-1
  • 사례 위험등급
    Class II
  • 사례 시작날짜
    2013-09-13
  • 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
    Carestream health australia has received reports from overseas of unusable diagnostic images on exams where a normal exposure mode (nem) view is exposed immediately prior to an extended exposure mode (eem) view with the system in fast preview mode.
  • 조치
    Carestream Health Australia is providing a firmware update that will allow NEM and EEM images to be taken in any order. The update will be provided at the next scheduled service or within 3 months. Until the firmware upgrade is installed end users are advised to only perform the EEM acquisition prior to the NEM acquisition.

Device

  • 모델명 / 제조번호(시리얼번호)
    DRX Revolution Mobile, DRX Mobile Retrofit & DRX Transportable X-ray SystemsAll lot numbers affectedARTG Numbers: 194055 & 161988
  • Manufacturer

Manufacturer