Device Recall VSign Membrane Changer 의 리콜

U.S. Food and Drug Administration에 따르면, 해당 리콜 는 United States 에서 Sentec AG 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
    63631
  • 사례 위험등급
    Class 2
  • 사례 연번
    Z-0434-2013
  • 사례 시작날짜
    2012-11-05
  • 사례 출판 날짜
    2012-11-22
  • 사례 상황
    Terminated
  • 사례 국가
  • 사례 종료 날짜
    2012-12-18
  • 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
    Monitor, carbon-dioxide, cutaneous - Product Code LKD
  • 원인
    A manufacturing defect was observed for the membrane changer insert that does not allow electrolyte to be present under the new membrane. the pco2 performance of a sensor without electrolyte will be deteriorated.
  • 조치
    SenTec notified the one US distributor via e-mail on November 5, 2012. The distributor was advised to stop distribution of affected lot numbers. The communication to the distributor described the issue, identified affected product, and stated that SenTec will replace current stock at the end-customer level. The end user can discard the affected products. The distributor is asked to respond back with an e-mail to SenTec that they took appropriate action.

Device

  • 모델명 / 제조번호(시리얼번호)
    Lot numbers: 1D0F, 1D58, 1D80, 1DCA, 1DEA, 1E5F
  • 의료기기 분류등급
  • 의료기기 등급
    2
  • 이식된 장치?
    No
  • 유통
    Distributed only in MO.
  • 제품 설명
    SenTec V-Sign Membrane Changer Insert (VS-MCI), 5 pieces. The SenTec V-Sign Membrane Changer Insert is indicated for use with the V-Sign Membrane Changer only. || The V-sign Sensor is indicated for use with the SenTec Digital Monitor when continuous non-invasive monitoring of carbon dioxide tension, oxygen saturation, and pulse rate are required for adult and pediatric patients.
  • Manufacturer

Manufacturer

  • 제조사 주소
    Sentec AG, Ringstrasse 39, Therwil, Baselland Switzerland
  • 제조사 모회사 (2017)
  • Source
    USFDA