Prestige 2, Prestilix, Prestige VH, Prestige SI, RFX/SFX, Legacy and Precision 500D, ADVANTX and Innova 2000 Systems(Diagnostic fluoroscopic x-ray systems) 의 리콜

Department of Health, Therapeutic Goods Administration에 따르면, 해당 리콜 는 Australia 에서 GE Healthcare Australia Pty 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-01602-1
  • 사례 위험등급
    Class II
  • 사례 시작날짜
    2016-12-09
  • 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
    There have been reported incidents of a distar crt monitor that has fallen off the monitor suspension related to product ageing. a fall of a crt monitor could result in a serious injury to a patient or operator. crt monitors, crt monitor feet, and crt suspensions systems have exceeded their nominal life and are obsolete.
  • 조치
    GE Healthcare will correct all affected products. A GE Healthcare representative will contact affected customers to arrange for the correction. In the interim, customers are advised of the following: - The CRT monitor & suspension should be inspected & used with caution. Make sure the monitors are secured properly to the tray before each use. Immediately stop using the system in case of any looseness of the monitor noticed contact your GE service representative. - Monitor should not be positioned directly above the patient. - Position the monitor by grasping the handle at the side or front of the tray & gently move to position as recommended in the User Manual 45-296411. - Before service / preventative maintenance of the monitor is attempted on a GE system by non-GE service personnel, GE strongly recommends that they obtain an updated copy of the service and preventive maintenance procedures from a GE Healthcare representative or download from the GE On-Line Documentation website.

Device

  • 모델명 / 제조번호(시리얼번호)
    Prestige 2, Prestilix, Prestige VH, Prestige SI, RFX/SFX, Legacy and Precision 500D, ADVANTX and Innova 2000 Systems(Diagnostic fluoroscopic x-ray systems)ARTG Number: 93871
  • Manufacturer

Manufacturer