VariSource iX Control Software 의 리콜

Department of Health, Therapeutic Goods Administration에 따르면, 해당 리콜 는 Australia 에서 Varian Medical Systems Australasia 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-2015-RN-01010-1
  • 사례 위험등급
    Class II
  • 사례 시작날짜
    2015-10-15
  • 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
    An anomaly has been identified with the varisource ix control software. in the event a forced logoff occurs while the dummy wire is extended during a treatment session, the partial fraction generated by the system will be incorrect. the control software does not differentiate the re-start dummy sweep from the dummy sweep at the beginning of the treatment session. the control software assumes no treatment has been delivered. the partial fraction generated will be equivalent to the original full fraction. if this partial fraction is treated, this would result in re-treatment of any dwell positions actually delivered prior to the session interrupt and result in a dose greater than intended. the treatment recovery report will incorrectly indicate that no dwell positions have been treated. both the treatment delivery report and the treatment history report do correctly indicate the dwell positions treated.There have been no reports of patient injury due to this issue.
  • 조치
    Varian Medical Systems is developing a technical correction for this issue. A Technical Service representative will contact the affected hospital when this correction is available to schedule its installation. In the interim a workaround is provided in the Customer Letter.

Device

  • 모델명 / 제조번호(시리얼번호)
    VariSource iX Control SoftwareAffected Versions/Lots: Version 1.2.1, Build 3726 and Version 1.2, Build 2.4336 ARTG Number: 119982
  • Manufacturer

Manufacturer