Events

NUTRILINE CATHETER WITH STYLET AND MICROFLASH 의 리콜

Health Canada (via FOI)에 따르면, 해당 리콜 는 Canada 에서 ADVANCED SURGI-PHARM/BATRIK MEDICAL MFG./IMPERIAL SURGICAL 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
    25935
  • 사례 위험등급
    III
  • 사례 시작날짜
    2017-07-12
  • 사례 국가
    Canada
  • 사례 출처
    HC
  • 비고 / 경고
    Canadian data is current through March 2018. All of the data comes from Health Canada, 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 Canada.
  • 데이터 추가 비고
  • 원인
    Two vygon nutriline kits are being recalled because it was found that they were packaged with an incorrect version of the microflash introducer. the version packaged in the affected product is a ce-marked version that is not yet cleared in the us or licensed in canada. the change of introducer insider the nutriline kits was made in error as the un-licensed introducer was not approved to be in the nutriline kits.

Device

NUTRILINE CATHETER WITH STYLET AND MICROFLASH

Manufacturer

ADVANCED SURGI-PHARM/BATRIK MEDICAL MFG./IMPERIAL SURGICAL LTD.
  • 제조사 주소
    DORVAL
  • Source
    HC