Vapotherm 의 리콜

U.S. Food and Drug Administration에 따르면, 해당 리콜 는 United States 에서 Vapotherm, Inc. 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
    69116
  • 사례 위험등급
    Class 2
  • 사례 연번
    Z-2700-2014
  • 사례 시작날짜
    2014-08-13
  • 사례 출판 날짜
    2014-09-25
  • 사례 상황
    Terminated
  • 사례 국가
  • 사례 종료 날짜
    2015-10-02
  • 사례 출처
    USFDA
  • 사례 출처 URL
  • 비고 / 경고
    U.S. data is current through June 2018. All of the data comes from the U.S. Food and Drug Administration, except for the category Manufacturer Parent Company.
    The Parent Company was added by ICIJ.
    The parent company information is based on 2017 public records.
  • 데이터 추가 비고
    Humidifier, respiratory gas, (direct patient interface) - Product Code BTT
  • 원인
    Disposable patient circuit that allows water to leak into the center gas lumen.
  • 조치
    Vapotherm issued an Initial Notification on August 13, 2014. The letter was updated on August 20, 2014 to include two additional lots. The recall letter notified users that this defect is easily detectable during normal use and the probability of serious injury or death is remote. The letter was sent to raise awareness of the recent increase in incidence rate of this issue and reminded users of the requirement in the operating manual that requires that the cannula be connected to the patient only after the set temperature is reached. The letter also advised patient care personnel not to use, or to discontinue use of any Disposable Patient Circuit if water is observed leaking into the center lumen or from the cannula. They were instructed to replace the device and report the defect to Vapotherm immediately for further investigation. Should you have any questions please contact our technical support team at Email: ts@vtherm.com (US) 855.557.8276 (INTL) 1-603.658.5121

Device

  • 모델명 / 제조번호(시리얼번호)
    Lot Numbers 1402021 through 1406010, excluding lots 1402024 through 1402028 and 1404003. These numbers are applicable regardless of the prefix preceding them (i.e. HF, HFE, HFH, HFN, LF, LFE, LFH or LFN).
  • 의료기기 분류등급
  • 의료기기 등급
    2
  • 이식된 장치?
    No
  • 유통
    Worldwide Distribution - USA (nationwide) and Internationally to Canada, France, Swizerland, Korea, Sweden, Germany , Belgium, Spain, Mexico, Scotland, UAE, Australia, Israel, Hong Kong, Ireland, kuwait, and Italy.
  • 제품 설명
    Vapotherm Precision Flow,Disposable Patient Circuit || PF-NODPC-Low. || For use with the Precision Flow system and Ikaria INOmax DSIR || ¿ System. || This DPC allows clinicians to administer nitric oxide non-invasively via high || flow nasal cannula. In the Precision Flow High Flow Therapy application, a || special disposable patient circuit re-routes the gas to the INOmax injector || module then back into the Precision Flow system
  • Manufacturer

Manufacturer

  • 제조사 주소
    Vapotherm, Inc., 22 Industrial Dr Ste 1, Exeter NH 03833-4557
  • 제조사 모회사 (2017)
  • Source
    USFDA