Apex (Multileaf collimator used with Elekta linear accelerators) 의 리콜

Department of Health, Therapeutic Goods Administration에 따르면, 해당 리콜 는 Australia 에서 Elekta 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-2013-RN-00083-2
  • 사례 위험등급
    Class I
  • 사례 시작날짜
    2013-01-30
  • 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
    If the apex collimator has not been correctly installed on the radiation head and the user use the touchguard button to override the touchguard inhibit and rotate the gantry, the apex collimator can disconnect form the radiation head. this can occur because a fault condition that shows that the apex collimator was not attached correctly is bypassed.
  • 조치
    Users are requested to include additional safety information provided with the customer letter in the instructions for use. The safety information requests users to ensure that they do not override the touchguard inhibit or rotate the gantry after installing the Apex collimator. The safety information also informs users that the View Restrictions dialogue box may not show the touchguard inhibit restriction if there are other restrictions present.

Device

  • 모델명 / 제조번호(시리얼번호)
    Apex (Multileaf collimator used with Elekta linear accelerators)ARTG Number: 186855
  • Manufacturer

Manufacturer