Siemens e.cam Systems (Nuclear medicine gamma camera) 의 리콜

Department of Health, Therapeutic Goods Administration에 따르면, 해당 리콜 는 Australia 에서 Siemens Healthcare 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-2015-RN-00657-1
  • 사례 위험등급
    Class I
  • 사례 시작날짜
    2015-07-17
  • 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 has received a report of unintended detector motion. the cause of this motion was determined to be the simultaneous failure of two components, the radial brake circuit and touch pad. this unique combination of failures caused the axis brake to be ineffective, which ultimately led to the detector motion. additionally, activating the emergency stop (e-stop) or a system power failure, between 0.05 and 0.1 seconds after initiating motion could lead to this failure. siemens has determined that the likelihood that these events would occur over such a small time window is extremely rare. the most likely condition that could lead to a rapid power cycling is a touch pad failure. there have been no reports of injury as a result of this issue; however, it is remotely possible that a compression injury to the patient could occur.
  • 조치
    -PRODUCT CORRECTION Siemens has designed and will install an improved brake control circuit which will correct this condition. Users are advised that the e-stop should still be used confidently and they can continue to use their system with confidence while waiting for the repair to be scheduled and performed. Users are reminded that daily touch test and/or its failure should not be ignored. If they experience difficulty or a failure while performing the daily touch pad test, discontinue use and contact their local service representative. This action has been closed-out on 05/09/2016.

Device

  • 모델명 / 제조번호(시리얼번호)
    Siemens e.cam Systems (Nuclear medicine gamma camera) Multiple catalogue numbers installed prior to December 31st 2004 affectedPart numbers: 4380213, 4380221, 5242826, 5977066, 5989079, 5991109, 5992099, 7324143, 7823946, 7823953. ARTG number: 186317
  • 의료기기 분류등급
  • Manufacturer

Manufacturer