Device Recall ABL 700 series analyzers 의 리콜

U.S. Food and Drug Administration에 따르면, 해당 리콜 는 United States 에서 Radiometer 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
    36812
  • 사례 위험등급
    Class 3
  • 사례 연번
    Z-1094-2007
  • 사례 시작날짜
    2006-11-13
  • 사례 출판 날짜
    2007-07-24
  • 사례 상황
    Terminated
  • 사례 국가
  • 사례 종료 날짜
    2012-05-09
  • 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
    blood gas analyzers - Product Code CHL
  • 원인
    Software anomaly. protein removing program incorporated in the operating software for versions: v3.833 and v5.24, of the abl700 and abl800 blood gas analyzers, may allow for protein build up on the electrode membranes of blood gas analyzers. this condition can influence analyzer results. when the protein removal program is run too frequently, more than once a week, or when running the protein rem.
  • 조치
    The firm issued a 'Safety Alert Notice' [FAN 915-248] to all customers which received the recalled ABL700 and ABL800 Analyzers equipped with the referenced software. The 11/13/2006 notice describes the problem concerning the Protein Removal program to the user/customers and emphasizes that the frequency of running the program in these software versions must be no more than once a week in order to prevent the protein build-up problem. It also contains additional recommendations for the user/customers for operation of these analyzer and informs the customers that a Radiometer Service Rep. will be coming out and making a software upgrade to these systems within the next few weeks. The alert notification is accompanied by a 'FAX FORM' to be signed and completed by each customer in order to verify that the alert notification has been received and that the staff members responsible for operating and maintaining the analyzer(s) on-site have been informed of this situation and that the necessary changes in the Operator's Manual concerning the Cleaning, Protein Removal, and Decontamination programs have been made.

Device

  • 모델명 / 제조번호(시리얼번호)
    All serial numbers of the ABL 700 series containing software version 3.833.
  • 의료기기 분류등급
  • 의료기기 등급
    2
  • 이식된 장치?
    No
  • 유통
    The recalled analyzers were distributed to customers nationwide throughout the U.S. and in some parts of Canada.
  • 제품 설명
    ABL 700 Series blood gas analyzers equipped with Software Version 3.833.
  • Manufacturer

Manufacturer

  • 제조사 주소
    Radiometer America Inc, 810 Sharon Dr, Westlake OH 44145-1598
  • Source
    USFDA