Symbia T Series and Symbia Intevo Camera System (SPECT/CT diagnostic imaging system) 의 리콜

Department of Health, Therapeutic Goods Administration에 따르면, 해당 리콜 는 Australia 에서 Siemens 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-00881-1
  • 사례 위험등급
    Class I
  • 사례 시작날짜
    2014-08-08
  • 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
    Siemens recently detected a rubber isolator with unfavourable aging properties. the function of this rubber isolator, which is situated within the rotate motor mounting assembly, may degrade over time and may impact motor support. in rare cases, when unfavourable aging has occurred, the rubber isolator may break and cause loss of support for the rotate motor. this event could lead to a rupture of the drive belt which in turn could damage the gantry covers and make contact with the patient. the possibility of a serious injury does exist if the belt makes contact with the patient. siemens have not received any reports of injury with the symbia t or symbia lntevo camera systems as a result of this problem.
  • 조치
    Customers are advised that they can continue to use the systems while waiting for the corrective action to be undertaken which includes new mounting plate with improved rubber components and a backup device to ensure trouble free operation in the future. If users are experiencing abnormal noise or vibration, they are advised to immediately discontinue use and asked to contact their service engineer. Users are also asked to ensure that the safety advisory is placed in the System Owner's Manual. This action has been closed-out on 15/07/2016.

Device

  • 모델명 / 제조번호(시리얼번호)
    Symbia T Series and Symbia Intevo Camera System (SPECT/CT diagnostic imaging system)Multiple catalogue numbers affectedARTG Number: 123883
  • 의료기기 분류등급
  • Manufacturer

Manufacturer