Brainlab Patient Data Manager(Used for the display of medical images or treatment / surgery plans from picture archiving and communication systems (PACS), file servers, or removable storage media) 의 리콜

Department of Health, Therapeutic Goods Administration에 따르면, 해당 리콜 는 Australia 에서 Brainlab Australia 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-2015-RN-00960-1
  • 사례 위험등급
    Class I
  • 사례 시작날짜
    2015-09-29
  • 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
    When actively deselecting a fused reference dataset in content manager (the default setting is “selected”), a contained point, object or trajectory may appear shifted and/or distorted in the subsequently used brainlab navigation or planning software. if a reference dataset is deselected and the error occurs, the magnitude of shift or distortion varies, depending on the differences between the two datasets. therefore, for some cases, the shift or distortion will be clearly visible when the plan is used in a brainlab planning or navigation system. however, a shift could also be non-obvious. if a shift or distortion occurred and was not detected during review of the data, the deviation of the information displayed in the brainlab planning or navigation software could mislead the user regarding clinical decisions. this could ultimately lead to ineffective treatment, serious injury or even death of the patient.
  • 조치
    Brainlab will provide a software solution to prevent the described scenario from occurring starting February 2016. In the interim, users are advised not to deselect individual datasets where a Point, Object or Trajectory was planned in. If users are unsure in which dataset a Point, Object or Trajectory was planned, do not deselect any content from the plan. Open the entire plan instead. Before patient treatment, always review the plausibility of all information input to and output from the device.

Device

  • 모델명 / 제조번호(시리얼번호)
    Brainlab Patient Data Manager(Used for the display of medical images or treatment / surgery plans from picture archiving and communication systems (PACS), file servers, or removable storage media)Product Version NumbersContent Manager (versions 2.0.0, 2.0.1, 2.0.2, 2.0.3, 2.1.0) Patient Browser (versions 4.0.0, 4.0.1, 4.0.2, 4.0.3, 4.1.0) DICOM Viewer (versions 2.0.0, 2.0.1, 2.0.2, 2.0.3, 2.1.0) ARTG Number: 96517
  • Manufacturer

Manufacturer