Magnetom Spectra 3.0 T System (MRI 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-00023-1
  • 사례 위험등급
    Class I
  • 사례 시작날짜
    2014-01-15
  • 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
    Due to an isolated production issue, the body coil in the mri may possibly be fatigued after certain months of usage. this fatigue may potentially lead to the risk of overheating during delivery of rf energy due to underestimated specific absorption rate (sar) in extremely rare conditions for head, neck and shoulder examinations. siemens is not currently aware of any incidents related to this issue. however, the risk of overheating which may include tissue damage cannot be totally excluded, although the possibility of occurrence for serious injury is extremely low according to siemens' risk assessment.
  • 조치
    Users are advised to undertake extra precautions during head, neck and shoulder scans ie, to advise patients to immediately communicate uncomfortable heating sensations so that the scan can be stopped. Body coils will be replaced as soon as possible for the systems which have been identified as having a slight beginning of aging. For the remaining potentially affected systems, tune up measurements and QA checks will be performed by the end of February 2014 to readjust the system if required to eliminate any immediate risk. All potentially affected body coils will be replaced by the end of May 2014.

Device

  • 모델명 / 제조번호(시리얼번호)
    Magnetom Spectra 3.0 T System (MRI system)Catalogue number: 10655588Serial numbers: 56031, 56029, 56019 & 56017ARTG number: 154128
  • Manufacturer

Manufacturer