Ingenuity TF PET/CT running software version 4.0.2 (4.0.0.26645) 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-2017-RN-01541-1
  • 사례 위험등급
    Class II
  • 사례 시작날짜
    2017-12-21
  • 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
    Philips has identified a software issue causing pet reconstructions to fail intermittently. it was determined that reconstructions fail due to a negative table position (-1 value is inserted) in the raw data list file, rather than the actual table position. this error has been found to occur in two scenarios resulting in acquisition data that will not be able to be reconstructed and will therefore be unusable: 1) when the system operator cancels an acquisition2) couch position requests within the software sequence were delayed a. the error occurs intermittently, but has been found to occur more frequently when the gantry’s network is heavily loaded with multiple retrospective reconstructions running in parallel. b.The error manifests to the technologist by an error message and failed status on the reconstruction monitor and the error message “result {0} failed to reconstruct” on the acquisition workflow window during reconstruction after the patient scan has been completed.
  • 조치
    It is recommended that the technologist follow the Warning provided in the Instructions for Use - System Information for Ingenuity TF 459800079321 Rev B, Section 2 Safety Guidelines, pg 2-17 and that the patient remains in the original scan position until reconstructed images are verified. Philips will be releasing a correction for this issue. A Philips Field Service Engineer will contact users to schedule the update.

Device

  • 모델명 / 제조번호(시리얼번호)
    Ingenuity TF PET/CT running software version 4.0.2 (4.0.0.26645)Model: 882442ARTG 292543
  • Manufacturer

Manufacturer

  • 제조사 모회사 (2017)
  • Source
    DHTGA