ACUSON S Family ultrasound systems with software versions VD10A or VD10C when using 18L6 HD transducer 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-2017-RN-00478-1
  • 사례 위험등급
    Class II
  • 사례 시작날짜
    2017-04-19
  • 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 a potential issue with the 18l6 hd transducer on the acuson s family ultrasound systems (with software versions vd10a or vd10). when scanning with the 18l6 transducer on the acuson helx evolution with touch control, the ultrasound system may display a triple image or an image with a dark band. when the triple image issue occurs, the system repeats one-third of the aperture, but does not display the full field of view. the issue occurs intermittently when connecting the 18l6 hd transducer to the ultrasound system or when selecting the touch screen control to activate the transducer. the potential risk is specific to breast exams and the possibility of not visualising lesions when acquiring images of breast tissue, which may result in a misdiagnosis.
  • 조치
    Siemens is recommending users perform the following steps before using the18L6 HD transducer: Connect the transducer to the ultrasound system and place a gel-coated fingertip on the transducer face. Drag the finger along the entire face of the transducer and if the echo from the finger displays in triplicate, disconnect and reconnect the transducer. Then repeat the test. It is recommended that users review any breast studies performed with an affected device to confirm no triple images were used as part of a diagnosis. Siemens is advising users that steps have been taken to resolve the issue with a software release.

Device

  • 모델명 / 제조번호(시리얼번호)
    ACUSON S Family ultrasound systems with software versions VD10A or VD10C when using 18L6 HD transducerCatalogue Numbers: S1000 – 10441701S2000 – 10041461S2000 (Refurbished) – 10440017S3000 – 1044173018L6 HD Transducer - 10041227 & 10789400ARTG Number: 137563
  • Manufacturer

Manufacturer