ARIA PRACTICE MANAGEMENT - 4D INTEGRATED TREATMENT CONSOLE (4DITC) 의 리콜

Health Canada (via FOI)에 따르면, 해당 리콜 는 Canada 에서 VARIAN MEDICAL SYSTEMS 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
    94139
  • 사례 위험등급
    II
  • 사례 시작날짜
    2012-05-17
  • 사례 국가
  • 사례 출처
    HC
  • 비고 / 경고
    Canadian data is current through March 2018. All of the data comes from Health Canada, 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 Canada.
  • 데이터 추가 비고
  • 원인
    When multiple conical collimator treatment plans are scheduled to be treated in a session the plan label should be displayed on the bccv dialog box should match the plan label on the 4ditc. however the name of the plan is not being updated correctly. all other identifiers including the accessory mount (conical collimator) are correct and are displayed correctly. a report was received involving the 4d integrated treatment console (4ditc) and bar - code conical collimator (bccv) indicating that the plan label is not updated correctly in bccv display if multiple plans are open in 4ditc simulatenously.

Device

  • 모델명 / 제조번호(시리얼번호)
    Model Catalog: V8.8 (Lot serial: H513769); Model Catalog: BCCV (Lot serial: HBC0210); Model Catalog: BCCV (Lot serial: HBC0028); Model Catalog: V8.8 (Lot serial: H515461)
  • 제품 설명
    ARIA PRACTICE MANAGEMENT - 4D INTEGRATED TREATMENT CONSOLE (4DITC)
  • Manufacturer

Manufacturer