Elekta Monaco Radiation Treatment Planning System 의 리콜

New Zealand Medicines and Medical Devices Safety Authority에 따르면, 해당 리콜 는 New Zealand 에서 Elekta Inc 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
    14991
  • 사례 시작날짜
    2013-07-12
  • 사례 국가
  • 사례 출처
    NZMMDSA
  • 사례 출처 URL
  • 비고 / 경고
    Data from New Zealand is current through July 2018. All of the data comes from the New Zealand Medicines and Medical Devices Safety Authority, 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 New Zealand.
  • 데이터 추가 비고
    Recalling Organisation: Elekta Pty Limited - New Zealand Branch, Level 2, Windsor Court , 128-136 Parnell Road, Parnell, AUCKLAND 1052
  • 원인
    Sample couch parameter files are supplied with monaco release 3.100 and later. the user can then access these files from the treatment couch library.By clicking on a particular couch file, the individual components of the couch can be selected and their densities edited. the user can then use the "save as treatment couch" to enter a unique name for the modified couch parameter file., when sample couch parameter files are edited, the densities altered, and "save" is selected, the sample files will be updated with these new, user defined densities. subsequently, when a software upgrade is loaded, the modified couch densities in these samples will be overwrittem with the default value of 1.000.
  • 조치
    Manufacturer to issue advice regarding use

Device

  • 모델명 / 제조번호(시리얼번호)
    Model: , Affected: , Software version: 3.100 and later
  • Manufacturer

Manufacturer