ACUSON SC2000 Ultrasound Systems 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-00005-1
  • 사례 위험등급
    Class II
  • 사례 시작날짜
    2014-01-03
  • 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
    The user interface module on the ultrasound system consists of the console (monitor, control panel and keyboard) and the swivel mechanism., the swivel mechanism is used for adjusting the height and rotation of the console and is attached to the column on the ultrasound system. if the connection of the user interface module to the column on the ultrasound system is lose, the entire module may fall off the ultrasound system. there is a potential risk of striking and harming anyone in the environment of the ultrasound system.
  • 조치
    End users are advised to inspect their units for any looseness in the attachment of the interface module to the column on the ultrasound system. If looseness is observed, discontinue use immediately and contact a Siemens service representative. A service engineer will perform the necessary repairs.

Device

  • 모델명 / 제조번호(시리얼번호)
    ACUSON SC2000 Ultrasound SystemsCatalogue Number: 10433816Serial Numbers lower than 401100ARTG Number: 139591
  • Manufacturer

Manufacturer