ACUSON S2000 DIAGNOSTIC ULTRASOUND SYSTEM - MAIN UNIT 의 리콜

Health Canada (via FOI)에 따르면, 해당 리콜 는 Canada 에서 SIEMENS CANADA LIMITED - HEALTHCARE 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
    68316
  • 사례 위험등급
    II
  • 사례 시작날짜
    2009-09-11
  • 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
    There is an intermittent series of events in which a print or store event failure may cause the following to occur: a)the last image of a patient study can be stored with the next new patient study performed. b)if the first patient's last image had measurement results will appear on the next patient's image. c) when a distance ratio or area ratio measurement is performed with l testis mass 2 measurement label it appears in the report as r testis mass 2 in english only and d) more than 4 measurements of the same label are performed will not apear on-screen or printed report.

Device

  • 모델명 / 제조번호(시리얼번호)
    Model Catalog: 10041461 (Lot serial: 200252); Model Catalog: 10041461 (Lot serial: 200995); Model Catalog: 10041461 (Lot serial: 200979); Model Catalog: 10041461 (Lot serial: 200926); Model Catalog: 10041461 (Lot serial: 200334); Model Catalog: 10041461 (Lot serial: 200288)
  • 제품 설명
    ACUSON S2000
  • Manufacturer

Manufacturer

  • 제조사 주소
    MISSISSAUGA
  • 제조사 모회사 (2017)
  • Source
    HC