Luminos dRF and Uroskop Omnia systems with Software Version VD10 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-2013-RN-01083-1
  • 사례 위험등급
    Class II
  • 사례 시작날짜
    2013-10-25
  • 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 identified the following potential malfunctions:1. during a rad (radiography) examination with automatic exposure control, a highly unlikely malfunction can result in radiation continuing longer than required. this malfunction happens when the generator stops the tube power too late and therefore too much dose is applied during an acquisition. this may also result in an overexposed image that is not of diagnostic quality, so that the examination needs to be repeated. (note: this issue also affects software versions vc10 and vb10. devices running this software are being corrected under recall rc-2013-rn-01037-1.)2. when selecting a tomo ogp, in some cases the luminos drf system shows a message "wait for flc" and this state does not change on its own.3. radiation is not activated and therefore an exposure is performed without radiation.
  • 조치
    It is not possible for the user to prevent this malfunction. The exposure time with the use of automatic exposure control is limited to 500ms, which is the maximum time that unwanted radiation will continue. The exposure can be interrupted by the user at anytime by releasing the exposure button. Siemens has implemented a field modification that will resolve the issues. The Australian roll out of this field modification is planned for completion in Q4 2013/Q1 2014.

Device

  • 모델명 / 제조번호(시리얼번호)
    Luminos dRF and Uroskop Omnia systems with Software Version VD10Catalogue Numbers:10094200, 10094910Siemens Reference Numbers: XP031/13/SARTG Number: 102184
  • Manufacturer

Manufacturer