Achieva 3.0T and Ingenia 3.0T MR Systems with passive shielding in the rear wall 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-01389-1
  • 사례 위험등급
    Class I
  • 사례 시작날짜
    2016-10-24
  • 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
    For the achieva 3.0t and ingenia 3.0t mr systems on sites with rear wall passive shielding, the thickness and location of shielding material must be installed according to requirements provided by philips. in cases where the requirements are not followed, the distance between the passive shielding rear wall and magnet could be insufficient. an insufficient distance leads to stronger attraction forces between the magnet and the passive shielding, which may lead to shearing of the magnet vibration pads. in a worst case scenario there may be displacement of the magnet, which could possibly result in harm (crushing risk) to persons inside the mr room and located between the magnet and passive shielding wall. to date there has been one overseas report of the magnet shifting with no harm to users or patients. displacement of a magnet can also result in image quality issues and mechanical fitting problems with the table. these functional issues affect the clinical usage of the mr system.
  • 조치
    Philips is advising customers that if the distance between magnet covers and finished rear wall is less than 1.3m, to contact Philips. In addition, Philips Field Service Engineers will be visiting all sites and checking this distance. If action is required, Philips will, as appropriate, replace the magnetic vibration pads and/or install seismic brackets. Depending on the circumstances, it may be advised that further clinical use of the MR system should not occur until after the installation corrections have been completed.

Device

  • 모델명 / 제조번호(시리얼번호)
    Achieva 3.0T and Ingenia 3.0T MR Systems with passive shielding in the rear wallARTG Number: 98887
  • Manufacturer

Manufacturer

  • 제조사 모회사 (2017)
  • Source
    DHTGA