Elekta X-ray Volume Imaging System (XVI), software versions 5.0.0 and 5.0.1 (Electronic Imaging Device (EID) used with radiation therapy treatment) 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-2014-RN-01187-1
  • 사례 위험등급
    Class I
  • 사례 시작날짜
    2014-11-11
  • 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 rare cases the xvi can incorrectly calculate the target position of the treatment table. the sequence of events when this error occurs is:- the user does an online volumeview acquisition and registration- the user accepts the registration and the table move assistant dialog box appearstwo different scenarios can result:- if the issue occurs only during initial patient set up the absolute actual column of the table move assistant dialog box incorrectly shows blank values. this error can cause a collision between the patient and the external beam limiting device but mistreatment cannot occur as it is not possible to get the table move assistant values in tolerance. - if the issue occurs at times other than initial patient set up the absolute actual column of the table movement dialog can display incorrect values. there is potential for clinical mistreatment if the relative set value is less than 01.Cm.
  • 조치
    Elekta is advising all affected users of the mandatory software upgrade which will prevent table movement if the start position has not been recorded correctly. A permanent solution for this problem is now available for all customers running XVI 5.0.0, XVI 5.0.1 systems. An Elekta service team member will contact the customers to install the software upgrade. This action has been closed-out on 07/06/2016.

Device

  • 모델명 / 제조번호(시리얼번호)
    Elekta X-ray Volume Imaging System (XVI), software versions 5.0.0 and 5.0.1 (Electronic Imaging Device (EID) used with radiation therapy treatment)ARTG number: 214673
  • Manufacturer

Manufacturer