Events

Vygon Umbilical Catheters 의 리콜

Department of Health, Therapeutic Goods Administration에 따르면, 해당 리콜 는 Australia 에서 Device Technologies Australia 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-2017-RN-01019-1
  • 사례 위험등급
    Class II
  • 사례 시작날짜
    2017-08-10
  • 사례 국가
    Australia
  • 사례 출처
    DHTGA
  • 사례 출처 URL
    https://apps.tga.gov.au/Prod/sara/arn-detail.aspx?k=RC-2017-RN-01019-1
  • 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
    The manufacturer vygon has identified a non-systematic wrong marking on specific vygon umbilical catheters. the first mark from the distal tip may be at 5.5cm instead of 4cm.
  • 조치
    Device Technologies is requesting customers: 1.Ensure all relevant personnel at their facility are fully informed of this notice, including medical staff who use Vygon Umbilical Catheters; 2.Quarantine all affected stocks remaining at their premises; and 3.Complete and return the supplied Reply Fax Form to acknowledge receipt of the notice and quantity of affected stock.

Device

Vygon Umbilical Catheters
  • 모델명 / 제조번호(시리얼번호)
    Vygon Umbilical CathetersProduct Code: VY-270.03 Batch Numbers: 241116FR, 281116FR, 071216FR, 151216FR, 211216FR, 050117FR, 230217FR, 280217FR, 060117FR and 150217FR ARTG Number: 141061
  • Manufacturer
    Device Technologies Australia Pty Ltd

Manufacturer

Device Technologies Australia Pty Ltd