PAD 300/PAD 300P Public Access Defibrillators (PAD) (Semi-automated defibrillator) 의 리콜

Department of Health, Therapeutic Goods Administration에 따르면, 해당 리콜 는 Australia 에서 Aero Healthcare 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-2012-RN-00974-1
  • 사례 위험등급
    Class I
  • 사례 시작날짜
    2012-11-02
  • 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
    1.The device may turn itself on without input from the user. when this occurs, the normal sequence of audible prompts will be emitted from the device. if this issue continues undetected, the battery will eventually become completely depleted below the minimum battery capacity necessary to allow for the delivery of therapy.2. certain devices may misinterpret a temporary drop in battery voltage as signalling low battery. this issue will result in the device prematurely displaying the low battery warning and turning itself off even if sufficient battery capacity remains. if the low battery warning is triggered due to this issue, the device will have sufficient power to deliver multiple shocks, but it is possible that the device will only deliver one shock before turning itself off. devices containing software version 1.4.2/ 3.2.0 or higher are not susceptible to this issue.
  • 조치
    Keep the devices in service. Follow the instructions from the sponsor to order a reserve battery pack and to download the new software. Aero Healthcare has advised the TGA that there are about 120 HeartSine PAD 300/PAD 300P units which could not be located during the recall. For more details, please see http://www.tga.gov.au/safety/alerts-device-heartsine-pad300-pad300p-131010.htm .

Device

  • 모델명 / 제조번호(시리얼번호)
    PAD 300/PAD 300P Public Access Defibrillators (PAD) (Semi-automated defibrillator)Affected serial numbers: 0400000501 to 0700032917, 08A00035000 to 10A0070753 & 10C00200000 to 10C00210318Manufactured between August 2004 and December 2010ARTG Number: 156690
  • 의료기기 분류등급
  • Manufacturer

Manufacturer