AIRIS II, Altaire Magnetic Resonance Imaging Devices 의 리콜

U.S. Food and Drug Administration에 따르면, 해당 리콜 는 United States 에서 Hitachi Medical Systems America 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
    35100
  • 사례 위험등급
    Class 2
  • 사례 연번
    Z-1104-06
  • 사례 시작날짜
    2006-04-28
  • 사례 출판 날짜
    2006-06-10
  • 사례 상황
    Terminated
  • 사례 국가
  • 사례 종료 날짜
    2008-11-24
  • 사례 출처
    USFDA
  • 사례 출처 URL
  • 비고 / 경고
    U.S. data is current through June 2018. All of the data comes from the U.S. Food and Drug Administration, except for the category Manufacturer Parent Company.
    The Parent Company was added by ICIJ.
    The parent company information is based on 2017 public records.
  • 데이터 추가 비고
    Magnetic Resonance Imaging MRI - Product Code LNH
  • 원인
    Software anomaly-a software defect can cause the slice line indicator to become mis-positioned during multi-planar reconstructions (mpr) with the potential for patient mis-diagnosis.
  • 조치
    The firm''s Field Service personnel will apprise the customers of this situation during scheduled visits at each customer location. During this visit, the corrected software will be installed by the Hitachi Field Service Technician. The installation of the software upgrades by the service technicians began on 4/28/2006. The firm anticipates that the correction of all units in their inventory as well as those units installed out-in-the-field will becompleted by 6/15/2006.

Device

  • 모델명 / 제조번호(시리얼번호)
    Serial Numbers: Altaire - L217, L219, L221, L224 and L225; AIRIS II - C686-C688* [*The AIRIS units remained in Hitachi's inventory and were not distributed].
  • 의료기기 분류등급
  • 의료기기 등급
    2
  • 이식된 장치?
    No
  • 유통
    The devices were distributed to five (5) customers located in four (4)states: Colorado, Ohio, Nebraska and Texas
  • 제품 설명
    AIRIS II, Altaire Nuclear Magnetic Resonance Imaging Device Systems
  • Manufacturer

Manufacturer

  • 제조사 주소
    Hitachi Medical Systems America Inc, 1959 Summit Commerce Park, Twinsburg OH 44087-2371
  • 제조사 모회사 (2017)
  • Source
    USFDA