Brilliance iCT and iCT SP, with software versions v4.1.3 and v4.1.5 의 리콜

Department of Health, Therapeutic Goods Administration에 따르면, 해당 리콜 는 Australia 에서 Philips Electronics Australia 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-2016-RN-00586-1
  • 사례 위험등급
    Class II
  • 사례 시작날짜
    2016-05-12
  • 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
    The following issues have been identified which may result in additional patient scanning & therefore additional radiation doses. there have been no reports of injuries as a result of these issues;- scan length changes with a change in the field of view (fov);- the doseright algorithm calculates a water equivalent diameter that is larger than measured on a cylindrical phantom when an 80 kvp or 120 kvp surview is used. this will result in a mas value for the scan that is higher than suggested when using a 100 kvp or 140 kvp surview. (note: the reported mas and ctdi values are correct for all scans & surviews);- wrong scan time estimation due to incorrect intergration time causes the surview scan near 184mm &135mm may result in unexpected scan start positions; &- there may be a discrepancy between the calculated reconstruction length & the actual scan length which may result in the inability to reconstruct the raw data. offline reconstruction of the raw data is also not possible.
  • 조치
    Philips is providing users with work around instructions to follow as an interim measure. A software upgrade will be implemented as a permanent correction.

Device

  • 모델명 / 제조번호(시리얼번호)
    Brilliance iCT and iCT SP, with software versions v4.1.3 and v4.1.5ARTG Number: 98868
  • Manufacturer

Manufacturer

  • 제조사 모회사 (2017)
  • Source
    DHTGA