Philips IntelliVue Information Center (PIIC) iX system (A Centralized Patient Monitoring System) 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-00077-1
  • 사례 위험등급
    Class I
  • 사례 시작날짜
    2015-01-30
  • 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
    Philips is informing that a software defect has been identified that involves the use of the “change bed label” feature at the information center ix. if the configuration for this item is set to “optional” and a user selects the “location” button within the “manage patient” menu and makes a change to the patient location, alarms for sp02 and/or non invasive blood pressure (nbp) will become disabled without visual notification (bell with an “x”) to the user. this problem only happens when the patient is monitored using a networked intellivue trx telemetry m4841/trx4851a patient worn device (pwd).
  • 조치
    Philips is providing instructions to the users to prevent this issue from occurring: Customers/users should: 1) Disable the Change Bed Label field in Patient Management. This is accomplished by changing the feature from ‘Optional to ‘Hidden’ 2) All patient transfers must be performed using the Transfer key in the Manage Patient application. Philips is providing a software correction to customers with impacted devices at no charge. This action has been closed-out on 08/08/2016.

Device

  • 모델명 / 제조번호(시리얼번호)
    Philips IntelliVue Information Center (PIIC) iX system (A Centralized Patient Monitoring System)Part Numbers: 866023 (IntelliVue Info Center iX), 866024 (PIIC iX Upgrade), 866117 (PIIC Classic Upgrade)Serial Numbers: Release A.00, A.01 and A.02 versions in use with M4841A/TRx4851 telemetry devicesARTG Number: 94237
  • 의료기기 분류등급
  • Manufacturer

Manufacturer

  • 제조사 모회사 (2017)
  • Source
    DHTGA