Philips IntelliVue MX40 Wearable Patient Monitors manufactured prior to the 6th of July 2015 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-2017-RN-00732-1
  • 사례 위험등급
    Class I
  • 사례 시작날짜
    2017-06-06
  • 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 has identified a higher than expected incidence of speaker failures, which results in the loss of audible alarms when the device is in monitor mode. the failure of the speaker results in the audio capabilities of the speaker being degraded and/or no sound at all. operation in telemetry mode is unaffected by speaker failure until disconnected from the information center, either intentionally or unexpectedly.Monitor mode: the mx40 provides local patient monitoring for a period limited by its battery life. the device will annunciate audible & visual alarms using the speaker & display on the mx40 when the alarm conditions are triggered. extended use in this mode raises the risk of the speaker failing.Telemetry mode: all alarming is automatically managed at the information center. mx40 speaker volume is set to zero & the display is off unless the user enables monitor mode. the device will automatically switch to monitor mode if it loses connection to the telemetry network.
  • 조치
    A Philips Healthcare representative will contact customers with affected devices to arrange for shipment of a replacement unit. The replacement device is currently manufactured with the improved hardware speaker design and latest software (includes speaker detection capability and INOP messaging) release. An interim workaround is also given in the Customer Letter until such time as the replacement can be made.

Device

  • 모델명 / 제조번호(시리얼번호)
    Philips IntelliVue MX40 Wearable Patient Monitors manufactured prior to the 6th of July 2015Product Number: 865351 Service Number: 453564262531 and 453564262551Product Number: 865352Service Number: 453564262571 and 453564262591Serial Numbers: lower than US03556362ARTG Number: 99204
  • 의료기기 분류등급
  • Manufacturer

Manufacturer

  • 제조사 모회사 (2017)
  • Source
    DHTGA