Device Recall IMPAX Agility 의 리콜

U.S. Food and Drug Administration에 따르면, 해당 리콜 는 United States 에서 AGFA Healthcare Corp. 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
    71606
  • 사례 위험등급
    Class 2
  • 사례 연번
    Z-2061-2015
  • 사례 시작날짜
    2015-06-26
  • 사례 출판 날짜
    2015-07-13
  • 사례 상황
    Terminated
  • 사례 국가
  • 사례 종료 날짜
    2016-01-27
  • 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
    System, image processing, radiological - Product Code LLZ
  • 원인
    Firm received a complaint that the hospital had sent two accession numbers over the same morning and on the agility side the patient name was incorrect.
  • 조치
    PRB0046372 was created to address the corrective actions related to this issue. On 6/26/2015, an email communication, as an effectiveness check was sent to the two customers. Acknowledgment, via email, that the communication was received was requested from the consignees.

Device

  • 모델명 / 제조번호(시리얼번호)
  • 의료기기 분류등급
  • 의료기기 등급
    2
  • 이식된 장치?
    No
  • 유통
    Distributed in the state of MO.
  • 제품 설명
    IMPAX Agility. || IMPAX Agility when deployed as a departmental Picture Archiving and communications system (PACS) provides an interface for the acquisition, display, digital processing, annotation, review, printing, storage and distribution of multimodality medical images, reports and demographic information for diagnostic purposes within the system and across computer networks.
  • Manufacturer

Manufacturer

  • 제조사 주소
    AGFA Healthcare Corp., 10 S Academy St, Greenville SC 29601-2632
  • 제조사 모회사 (2017)
  • Source
    USFDA