Philips IntelliVue Patient Monitors and Philips Avalon Fetal MonitorsIntelliVue Patient Monitors, software versions J.21.03 & J.21.19 의 리콜

Department of Health, Therapeutic Goods Administration에 따르면, 해당 리콜 는 Australia 에서 Philips Electronics Australia Ltd 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
    RC-2014-RN-01163-1
  • 사례 위험등급
    Class I
  • 사례 시작날짜
    2014-10-29
  • 사례 국가
  • 사례 출처
    DHTGA
  • 사례 출처 URL
  • 비고 / 경고
    Australian data is current through July 2018. All of the data comes from the Australian Therapeutic Goods Administration, 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 Australia.
  • 데이터 추가 비고
  • 원인
    In time-synchronized automatic/sequence mode the noninvasive blood pressure (nbp) automatic measurement series is stopped inadvertently, if the repetition interval is increased manually by the user (e.G. from 5 to 15 minutes) in between two consecutive measurements.- a prompt message “any ongoing nbp measurement and automatic cycle stopped” is displayed and a single tone sounds when the measurement series is stopped.- after the automated measurement series has been stopped, nbp numeric, repetition time, and time to next measurement are no longer displayed, i.E. the nbp numeric field is blank.If the nbp measurement is stopped, and a patient’s blood pressure is not being monitored, a delay in treatment could occur.
  • 조치
    A Philips Healthcare representative will contact customers with affected devices to arrange a software upgrade to correct the issues. During the interim period until the SW is upgraded, customers are advised to make sure, if the NBP repetition interval needs to be increased (e.g. from 5 to 15 minutes), to restart the automatic NBP measurement. This action has been closed-out on 12/08/2016.

Device

  • 모델명 / 제조번호(시리얼번호)
    Philips IntelliVue Patient Monitors and Philips Avalon Fetal MonitorsIntelliVue Patient Monitors, software versions J.21.03 & J.21.19Models and Product Numbers: MP5 (M8105A), MP5SC (M8105AS), MP5T (M8105AT), MP5 Upgrade (M8105AU), MP5SC Upgrade (866327)ARTG Number: 94238Avalon Fetal Monitors, software version J.30.58Models and Product Numbers: FM20 (M2702A), FM30 (M2703A), FM50 (M2705A)ARTG Number: 99202
  • 의료기기 분류등급
  • Manufacturer

Manufacturer

  • 제조사 모회사 (2017)
  • Source
    DHTGA