Events

Device Recall REGIUS IM, RIM 의 리콜

U.S. Food and Drug Administration에 따르면, 해당 리콜 는 United States 에서 Konica Minolta Medical Imaging USA, 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
    34785
  • 사례 위험등급
    Class 2
  • 사례 연번
    Z-0862-06
  • 사례 시작날짜
    2006-02-06
  • 사례 출판 날짜
    2006-05-16
  • 사례 상황
    Terminated
  • 사례 국가
    United States
  • 사례 종료 날짜
    2008-08-22
  • 사례 출처
    USFDA
  • 사례 출처 URL
    https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfres/res.cfm?id=44641
  • 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
    System, Image Processing, Radiological - Product Code LLZ
  • 원인
    If the patient demographic data is entered into the cs-1 manually, and the user fails to enter any data in one of the demographic data fields labeled as birthday, sex, name or patient comments, etc, the rim will populate the fields where no data has been entered with data from the previous patient.
  • 조치
    The firm phoned the customers on 2/6/2006 to inform them of the recall and the corrective action associated to the recall. This will be followed up with a fax, e-mail and letter. The final step will be visiting the location to install the correct software.

Device

Device Recall REGIUS IM, RIM
  • 모델명 / 제조번호(시리얼번호)
    58 units distributed between June 2003 and January 2006. Software version prior to January 31, 2006.
  • 의료기기 분류등급
    Radiology Devices
  • 의료기기 등급
    2
  • 이식된 장치?
    No
  • 유통
    The units were distributed to hospitals nationwide through the firm''s sales force and resellers. There are no government accounts.
  • 제품 설명
    REGIUS Image Manager (AKA REGIUS IM, RIM). Catalogue Number 5900554. Centralized CR Image Quality Control. Patient throughput optimization via offloaded processing from various CR readers. Technologist review and audit. Key processing for specialized exams, totally automated processing for hands off operation. Centralized workflow device for dispersed readers environments. HIS/RIS patient status updates. Demographic Correction.
  • Manufacturer
    Konica Minolta Medical Imaging USA, Inc.

Manufacturer

Konica Minolta Medical Imaging USA, Inc.
  • 제조사 주소
    Konica Minolta Medical Imaging USA, Inc., 411 Newark Pompton Tpke, Wayne NJ 07470-6657
  • Source
    USFDA