On-Board Imager (OBI) (used with linear accelerators for verification of correct patient position in relation to isocenter and verification of treatment fields) 의 리콜

Department of Health, Therapeutic Goods Administration에 따르면, 해당 리콜 는 Australia 에서 Varian Medical Systems Australasia 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-2014-RN-00363-1
  • 사례 위험등급
    Class I
  • 사례 시작날짜
    2014-03-26
  • 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
    In the three known failures, belt over-tensioning caused the motor shaft to fail over time. this over tensioning would have taken place during servicing. this failure permitted the exact arm elbow joint to swing freely with gravity. a message such as "kv detector elbow axis not calibrated" or "kv source elbow axis not calibrated" may appear, or the user may hear a grinding or shearing sound at or before the time of failure. potential injury from the kv source striking a patient is dependent upon the anatomic site being treated and the height of the couch.
  • 조치
    A Varian Medical Systems Customer Support Service representative will arrange a site visit to check the belt tension of the Type 01 elbow motors of all OBI and MV Exact arms. If over-tensioned belts are detected, the elbow motor will be replaced with a Type 02 elbow motor. Until Varian inspects the OBI Exact arms, users should not extend or retract the kV Source arm when it is above a patient. Users should ensure that the gantry is positioned so that the kV Source is lateral to, or underneath, the patient-couch prior to extending or retracting the arm. Sites doing their own servicing or using a third party service provider, must ensure that they are following Varian service instructions. This action has been closed-out on 02/02/2016.

Device

  • 모델명 / 제조번호(시리얼번호)
    On-Board Imager (OBI) (used with linear accelerators for verification of correct patient position in relation to isocenter and verification of treatment fields)ARTG Number: 117950
  • 의료기기 분류등급
  • Manufacturer

Manufacturer