Events

Bard 2-Way Foley Catheters and 2-Way Council Tip Foley Catheters 의 리콜

New Zealand Medicines and Medical Devices Safety Authority에 따르면, 해당 리콜 는 New Zealand 에서 C R Bard 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
    19606
  • 사례 시작날짜
    2016-01-07
  • 사례 국가
    New Zealand
  • 사례 출처
    NZMMDSA
  • 사례 출처 URL
    https://medsafe.govt.nz/hot/Recalls/RecallSearch.asp
  • 비고 / 경고
    Data from New Zealand is current through July 2018. All of the data comes from the New Zealand Medicines and Medical Devices Safety Authority, 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 New Zealand.
  • 데이터 추가 비고
    Recalling Organisation: Pharmacy Retailing (NZ) Ltd t/a Healthcare Logistics, 54 Carbine Road, Mt Wellington, AUCKLAND
  • 원인
    Manufacturer has identified that the instructions for use (ifu) included with the products listed in attachment #1 distributed from june 2013 to june 2015 provide the incorrect inflation volume. the inflation volume provided on the catheter's valve cap does state the correct inflation volume. the ifu contains a chart entitled recommended inflation volumes with incorrect volumes.
  • 조치
    Instructions for use to be updated

Device

Bard 2-Way Foley Catheters and 2-Way Council Tip Foley Catheters
  • 모델명 / 제조번호(시리얼번호)
    Model: 0165SI08, 0165SI10, 0165SI12, 0165SI14, 0165SI16, 0165SI18, 0165SI20, 0165SI22, 0165SI24, 0165SI26, 0165SI28,0165SI30 0196SI16.0196SI18, 0196SI20 and 0196SI22, Affected:
  • Manufacturer
    C R Bard Inc

Manufacturer

C R Bard Inc