Philips HeartStart MRx Monitor/Defibrillator 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-00401-1
  • 사례 위험등급
    Class I
  • 사례 시작날짜
    2017-03-27
  • 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
    The possibility of abnormal device behaviours has been identified in the heartstart mrx monitor/defibrillator. the device may exhibit the following issues:1. if the battery connecting pins (in the battery compartment of the heartstart mrx monitor/defibrillator) become damaged or contaminated, it could result in a poor electrical connection that may cause the mrx to either (i) not power on or (ii) repetitively reboot, when used on battery power only 2. after unplugging the device from ac mains, there are two abnormal behaviours of the heartstart mrx monitor/defibrillator that may occur:a) after the user depresses the charge button, the device attempts to charge, and after approximately 20 seconds, generates the “shock equipment malfunction” error message and is unable to deliver shock therapy.B) pacing may cease without warning. these device behaviours continue until the unit is reset.Either problem could potentially delay monitoring or therapy.
  • 조치
    Philips is advising customers to take the following corrective actions: Issue 1, inspect the HeartStart MRx battery compartment connections on the device. Include this step as part of a routine Operational Check to verify that the battery connector pins are clean, fully extended, not bent, and without residue; and Issue 2, if the External Power Indicator light above the MRx display remains illuminated after the device is unplugged from AC mains power, leave the device unplugged, remove and reinsert the battery and confirm that the Indicator has turned off. Customers are requested to refer to their recall notification letter for further important details.

Device

  • 모델명 / 제조번호(시리얼번호)
    Philips HeartStart MRx Monitor/DefibrillatorModel Numbers: M3535A, M3536A, and military bundles Units: M3535A (M3535ATZ)M3536A (M3536ATZ)M3536M, M3536MCM3536M2, M3536M3, M3536M4, M3536M5, M3536M6, M3536M7, M3536M8, M3536M9
  • 의료기기 분류등급
  • Manufacturer

Manufacturer

  • 제조사 모회사 (2017)
  • Source
    DHTGA