IntelliSpace PACS 4.4 (Radiology picture archiving and communication system) 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-00952-1
  • 사례 위험등급
    Class I
  • 사례 시작날짜
    2014-09-02
  • 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
    In philips intellispace pacs 4.4, there is feature which allows the optional configuration of auto export of resolved study exception immediately after resolution. when this configuration is used, it is possible for a system timing issue to occur when exporting data to 3rd party devices. if this system timing issue occurs when demographics are updated, such as during exception resolution and the study is immediately exported, the patient demographic information can be incorrect in the exported data. although the data is correct in intellispace pacs if diagnosis is performed on this exported data using a 3rd party device the user may not be aware of unchanged patient data is being utilised. if this were to occur diagnosis may be based on an incomplete set of images, or images that are associated with the wrong patient. the hazard involved is that diagnosis may be based on an incomplete set of images, or images that are associated with the wrong patient.
  • 조치
    Each site will be contacted by Philip’s Technical Account Manager and notified if Auto Export is configured at the site and to schedule either the disabling or the correction of the Auto Export Feature. Determined by site utilization of the feature, Philips will schedule and deploy software correction or will disable the Auto Export Feature for all IntelliSpace 4.4 installations impacted by this issue. This action has been closed-out on 17/08/2016.

Device

  • 모델명 / 제조번호(시리얼번호)
    IntelliSpace PACS 4.4 (Radiology picture archiving and communication system)All versions of IntelliSpace PACS 4.4 with Auto Export Feature Enabled are affectedARTG Number: 178437
  • 의료기기 분류등급
  • Manufacturer

Manufacturer

  • 제조사 모회사 (2017)
  • Source
    DHTGA