ISOLINE 2CR6 and 2CT6 Implantable Defibrillation Leads 의 리콜

Department of Health, Therapeutic Goods Administration에 따르면, 해당 리콜 는 Australia 에서 Sorin Group Australia 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-2013-RN-00088-2
  • 사례 위험등급
    Class I
  • 사례 시작날짜
    2013-01-31
  • 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
    As of december 31, 2012, 30 cases of internal insulation breach under the rv or svc defibrillation coil have been confirmed by the analysis conducted on returned products. in each of the 30 identified cases, the internal insulation breach of the silicone lumen was observed under the rv and/or svc defibrillation coil, i.E. where the microcables are not coated with etfe, resulting in a contact between the conductors, thus leading to low pacing impedance and/or ventricular oversensing, and/or inappropriate therapy. it should be noted that in case of ventricular oversensing, pacing is inhibited.
  • 조치
    Sorin Group Australia is issuing a 'Hazard Alert' letter to implanting/ treating clinicians and hospitals detailing the issues and how to manage the affected patients. The TGA has published a web statement regarding the issues. For more information, please see http://www.tga.gov.au/safety/alerts-device-isoline-leads-130306.htm .

Device

  • 모델명 / 제조번호(시리얼번호)
    ISOLINE 2CR6 and 2CT6 Implantable Defibrillation LeadsPrevious ARTG numbers (cancelled in Nov 2011) : 165673, 165674Multiple serial numbers
  • 의료기기 분류등급
  • Manufacturer

Manufacturer