OEC 9800, OEC UroView 2800, OEC MiniView 6800, OEC FlexiView 8800 (mobile flouroscopic x-ray diagnostic system)Systems supplied in Australia:System: OEC 9800 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-2014-RN-01072-1
  • 사례 위험등급
    Class I
  • 사례 시작날짜
    2014-10-03
  • 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 are potential safety issues due to part replacements associated with certain components as follows: safety issue #1: the workstation cover may be able to be removed without the use of a tool. if the workstation front cover is removed, the user could be exposed to high voltage resulting in an electric shock. safety issue #2: surge suppressor board may have been replaced with an earlier revision. if the surge suppressor board is subjected to high voltage surges, damage to surge suppressor board components may occur and prevent the system from booting.Safety issue #3: solid state drive may have been replaced with a magnetic hard disk drive. the magnetic hard disk drive is more susceptible to data corruption that may prevent the system from booting.Safety issue #4: workstation power cable may have been replaced with an earlier revision which contains an unnecessary connection that could be subject to a potential connection failure, and prevent the system from booting.
  • 조치
    A GE Healthcare Field Engineer will contact customers to coordinate an inspection of the affected part/s, replacement of the affected part/s if necessary, and will ensure that systems meet the specifications. Work around instructions have been provided in the interim for each of the safety issues identified above. This action has been closed-out on 07/06/2016.

Device

  • 모델명 / 제조번호(시리얼번호)
    OEC 9800, OEC UroView 2800, OEC MiniView 6800, OEC FlexiView 8800 (mobile flouroscopic x-ray diagnostic system)Systems supplied in Australia:System: OEC 9800Serial Number: 86-1220Sysem: OEC 6800Serial Number: 89-2550ARTG Number: 132698
  • Manufacturer

Manufacturer