HeartWare HVAD Controller AC Adapter and HeartWare HVAD Battery 의 리콜

Department of Health, Therapeutic Goods Administration에 따르면, 해당 리콜 는 Australia 에서 Heartware Pty 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-01261-1
  • 사례 위험등급
    Class I
  • 사례 시작날짜
    2016-01-07
  • 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
    Heartware ac adapters with serial numbers cac000001 to cac005796 are vulnerable to power grid surges above 220 volts. if an ac adapter fails, the patient’s controller will alarm and automatically switch to the other power source. if patients follow heartware’s patient manual, there are no elevated risks to health. however, if a patient is not connected to two power sources, or if the second power source is insufficient to power the system during the time that it takes to replace a failed ac adapter, the system could lose power, which may lead to serious injury or death.In addition, there have been complaints related to earlier than expected battery depletion for batteries with serial numbers bat000001 to bat199999. premature or unrecognised battery depletion may pose a risk to the patient, if the patient is not connected to two power sources, or if the second power source is insufficient to power the system during the time that it takes to replace a depleted battery.
  • 조치
    The sponsor is advising healthcare professionals to identify and quarantine the affected units in hospital inventory and arrange for current patients to bring their AC Adapters and Batteries to a clinic as soon as possible (at least within the next three months), with urgency dependent upon individual patient circumstances. During their scheduled appointment, a qualified representative will assist with the quarantine and replacement of the affected product. For further information, please see http://www.tga.gov.au/alert/heartware-ventricular-assist-device-ac-adapters-and-batteries .

Device

  • 모델명 / 제조번호(시리얼번호)
    HeartWare HVAD Controller AC Adapter and HeartWare HVAD BatteryController AC Adapter Product Code: 1430XXSerial Numbers: CAC000001 to CAC005796 HVAD BatteryProduct Code: 1650XX and A00035 Serial Numbers: BAT000001 to BAT199999ARTG Number: 181875
  • Manufacturer

Manufacturer

  • 제조사 모회사 (2017)
  • 제조사 의견
    “If our surveillance systems identify a potential performance issue, our personnel promptly evaluate the problem, including, when appropriate, conducting root cause investigations and internal testing to assess whether the product continues to meet specifications and defined performance criteria,” Medtronic told ICIJ in a statement. “In some cases, based on this evaluation, Medtronic may determine that a recall is necessary.” The company said that it communicates with healthcare providers and/or patients and provide recommendations to address such issues. Medtronic noted that these communications can include letters, emails, calls, press releases, physician notifications and social media postings, as well as informing the FDA and other regulators of the actions.
  • Source
    DHTGA