IntelliSpace Portal, software versions 5.0.0, 5.0.1, 5.0.2, 6.0.0, 6.0.1, 6.0.2(Processes clinical images from different imaging modalities i.e., CT, NM, MR and enables advanced visualisation) 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-2014-RN-00977-1
  • 사례 위험등급
    Class I
  • 사례 시작날짜
    2014-09-11
  • 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 could lead to misdiagnosis which may result in patient mistreatment:1. when reopening a bookmark generated from processing a muga (multi-gated acquisition) scan within the nm cardiac application, the ejection fraction (ef) displayed may be different from the ef originally displayed when the bookmark was first created. 2. when processing using autoquant, emory cardiac toolbox, corridor4dm, or neuroq nm clinical applications, the patient study presented to the reviewing physician may be for a different patient than the one selected from the patient directory. 3. while using the nm viewer application, an arrow annotation added to a display moves away from its original position if the viewer is maximised or if the image is zoomed in or out. 4. while displaying pet images within ct viewer, the suv results displayed are different from the one specified in system preferences. this issue affects the ct viewer and multi-modality tumour tracking applications.
  • 조치
    Philips Healthcare is providing users with temporary workarounds in the customer letter for the identified problems. The issues have been corrected in software versions 5.0.2.3 and 6.0.2.3. Philips Service Engineer will contact the customers for implementation of the software update on the affected systems. This action has been closed-out on 9/08/2016.

Device

  • 모델명 / 제조번호(시리얼번호)
    IntelliSpace Portal, software versions 5.0.0, 5.0.1, 5.0.2, 6.0.0, 6.0.1, 6.0.2(Processes clinical images from different imaging modalities i.e., CT, NM, MR and enables advanced visualisation)Models:IntelliSpace Portal DX/HX/EX IntelliSpace Portal IXIntelliSpace Portal LX SPECTARTG Number: 188684
  • Manufacturer

Manufacturer

  • 제조사 모회사 (2017)
  • Source
    DHTGA