Device Recall Philips eCareManager System 의 리콜

U.S. Food and Drug Administration에 따르면, 해당 리콜 는 United States 에서 Visicu, 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
    61328
  • 사례 위험등급
    Class 2
  • 사례 연번
    Z-1474-2012
  • 사례 시작날짜
    2012-02-22
  • 사례 출판 날짜
    2012-04-27
  • 사례 상황
    Terminated
  • 사례 국가
  • 사례 종료 날짜
    2012-07-06
  • 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,network and communication,physiological monitors - Product Code MSX
  • 원인
    Three versions of software for the ecaremanager failed to display anticoagulants on the medications screen. the problem arose due to an unexpected change in the national drug data file.
  • 조치
    Philips notified all affected customers via a preliminary email message advising them of the issue. An URGENT - Field Safety Notice follow-up letter was mailed to all customers on February 22, 2012. This letter identified the affected product, described the problem and circumstances in which it can occur; recommend actions the customer should take to prevent risks for patients, and list the actions planned by Philips to correct the problem. For questions contact Philips eICU Customer Support 877-374-2872.

Device

  • 모델명 / 제조번호(시리얼번호)
    v3.7, v3.7.1, v3.8
  • 의료기기 분류등급
  • 의료기기 등급
    2
  • 이식된 장치?
    No
  • 유통
    Nationwide Distribution (USA) including states of MA, MO, WI, AR, AZ, PA, SD, VA, and IN.
  • 제품 설명
    Philips eCareManager System, Model 865325, software versions 3.7, 3.7.1 and 3.8. || Product Usage: The Philips eCareManager System software is intended for use in data collection, storage, and clinical information management with independent bedside devices and ancillary systems that are connected either directly or through networks. The eCareManager system provides patient information and surveillance of monitored patients at the point of care location and at a remote, supplementary care location through wide area networking technology and dedicated phone lines and is solely intended for use in a hospital environment. It is not intended to be used in a home environment.
  • Manufacturer

Manufacturer

  • 제조사 주소
    Visicu, Inc., 217 E Redwood St Ste 1900, Baltimore MD 21202-3315
  • 제조사 모회사 (2017)
  • Source
    USFDA