SPECTRUM INFUSION PUMP WITH MASTER DRUG LIBRARY 의 리콜

Health Canada (via FOI)에 따르면, 해당 리콜 는 Canada 에서 BAXTER CORPORATION 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
    15164
  • 사례 위험등급
    II
  • 사례 시작날짜
    2015-03-11
  • 사례 국가
  • 사례 출처
    HC
  • 비고 / 경고
    Canadian data is current through March 2018. All of the data comes from Health Canada, except for the categories Manufacturer Parent Company and Product Classification.
    The Parent Company and the Product Classification were added by ICIJ.
    The parent company information is based on 2017 public records. The device classification information comes from FDA’s Product Classification by Review Panel, based on matches of recall data from the U.S. and Canada.
  • 데이터 추가 비고
  • 원인
    Baxter has identified a discrepancy between the loading/bolus default dose settings in the master drug library (mdl) version 8.0 and the values displayed on the pump during loading/bolus dose programming. when a drug's loading dose or bolus dose is configured in the mdl with a default starting time value in seconds the loading dose or bolus dose setup screen on the pump will display the time value rounded to the nearest integer in minutes. when this occurs the pump will administer drugs as configured. this discrepancy is only with the default time on the setup screen not with the amount or rate of drugs administered as configured in the drug library.

Device

  • 모델명 / 제조번호(시리얼번호)
    Model Catalog: 35700BAX2 (Lot serial: >100 NUMBERS CONTACT MFR)
  • 제품 설명
    SPECTRUM INFUSION WITH MDL VERSION 8.0
  • Manufacturer

Manufacturer