Ysio Max, Luminos dRF Max, Luminos Agile Max, Uroskop Omnia Max with software version VE10A to VE10C 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-00992-1
  • 사례 위험등급
    Class II
  • 사례 시작날짜
    2014-09-15
  • 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
    Loss of images - if an automatic ris worklist update is performed while a patient is already selected for examination, the subsequently acquired images of this patient might get lost under certain circumstances and cannot be recovered. this malfunction is not detectable to the user during the examination. only after the patient study is opened in the “examined patients” list, the user will be able to recognize that the acquired images are not available and irreversibly lost.Incorrect labels and annotations - under certain circumstances the image label (l, r) and annotations are displayed incorrectly after images have been sent to pacs or hardcopy/filming.
  • 조치
    Siemens are working on a software update to correct both malfunctions. In the interim Siemens is providing the following work around instructions: - To avoid the potential risk of lost images Siemens is advising their customers to disable the automatic RIS worklist update and perform this procedure manually. - To ensure the correct orientation of images Siemens recommends to always use lead letters to indicate patient orientation on the x-ray image. This action has been closed-out on 06/06/2016.

Device

  • 모델명 / 제조번호(시리얼번호)
    Ysio Max, Luminos dRF Max, Luminos Agile Max, Uroskop Omnia Max with software version VE10A to VE10CARTG numbers – 102184, 102182
  • Manufacturer

Manufacturer