IntelliVie Information Centre (PIIC) iX (centralised patient monitor) 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-2015-RN-01226-1
  • 사례 위험등급
    Class I
  • 사례 시작날짜
    2015-12-16
  • 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
    Calculated ecg leads, also referred to as reconstructed leads when viewed or printed at the information center ix, may misrepresent the ecg waveform morphology in some reconstructed leads. (the full set of six limb leads is commonly calculated from 2 limb leads.)following are the lead combinations that are affected.· lead i and lead iii-(avl incorrectly reconstructed)· lead i and lead avr-(avl lead incorrectly reconstructed)· lead iii and lead avf-(ii incorrectly reconstructed)with this combination and hexad on, the 4 derived v leads morphology will also be misrepresented in review applications.Trx/mx40 only – iii, v or avr, v (avl incorrectly reconstructed) review applications only.
  • 조치
    Philips will be providing a software upgrade as a permanent correction. In the interm, users are informed that: - Arrhythmia alarms are not affected. ST alarms, ST values and measurements are also not affected and could be used to assist with the decision to obtain a diagnostic ECG. - The ECG waves at the bedside are not affected. Printing ECG waves from the bedside is an alternative to printing from the PIIC iX. Users are also advised that the most reliable method of patient monitoring combines close personal surveillance with correct operation of monitoring equipment.

Device

  • 모델명 / 제조번호(시리얼번호)
    IntelliVie Information Centre (PIIC) iX (centralised patient monitor)Affected Systems:866023 IntelliVue Information Centre iX, A.0866389 IntelliVue Information Centre iX, B.0866117 PIIC Classic UpgradeARTG Number: 94237
  • 의료기기 분류등급
  • Manufacturer

Manufacturer

  • 제조사 모회사 (2017)
  • Source
    DHTGA