Shimadzu Ceiling Type X-ray Tube Support 의 리콜

Department of Health, Therapeutic Goods Administration에 따르면, 해당 리콜 는 Australia 에서 Shimadzu Medical Systems Oceania 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-2017-RN-00698-1
  • 사례 위험등급
    Class II
  • 사례 시작날짜
    2017-06-08
  • 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 x-ray tube assembly in these devices is mounted to a tube mounting flange, which is part of the tube holding shaft. it was found that, extremely infrequently, a crack may occur over time on the tube holding shaft near the base of the tube mounting flange. if these cracks occur and then increase in size, the tube mounting flange may separate from the tube holding shaft. should separation of the tube mounting flange from the tube holding shaft occur, there is a risk that the x-ray tube assembly may come into contact with the patient or operator.
  • 조치
    Shimadzu will be contacting users to arrange for installation of additional protection parts to the x-ray tube support by a Shimadzu technical support engineer, to prevent the x-ray tube assembly from coming into contact with the patient or operator should separation of the tube mounting flange from the tube holding shaft occur. In the interim, users are advised to take the following actions: - Carry out daily inspection of the CH-200/CH-200 M as per instruction manual. - If abnormalities are found, such as rattling and/or deviation of the light irradiation field, discontinue use and contact the service representative. - When rotating the X-ray tube device, control the movement of the X-ray tube assembly to avoid a forceful stop at the end of the rotational movement. In the unlikely event that cracks have already occurred, a forceful stop at the end of rotational movement may accelerate cracking.

Device

Manufacturer