VenoCath Drum Cartridge Catheter (intravascular catheter) 의 리콜

Department of Health, Therapeutic Goods Administration에 따르면, 해당 리콜 는 Australia 에서 Hospira Pty Limited 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-2012-RN-00959-1
  • 사례 위험등급
    Class I
  • 사례 시작날짜
    2012-09-25
  • 사례 국가
  • 사례 출처
    DHTGA
  • 사례 출처 URL
  • 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.
    ICU Medical, Inc. acquired from Pfizer in early 2017, Hospira Infusion Systems, the portion of Hospira dedicated to develop infusion pumps.
  • 데이터 추가 비고
  • 원인
    Hospira has received reports from customers of drum cartridge catheter reports of the drum catheter dismantling/uncoiling before or during use/insertion. there have been complaints related to difficulty in inserting the catheter, leaks and separations, breakage of the catheter inside patient during insertion.
  • 조치
    Hospira is asking customers to immediately quarantine and return the affected stock for credit. Hospira is not going to continue to supply this product and is suggesting customer identify alternative products.

Device

  • 모델명 / 제조번호(시리얼번호)
    VenoCath Drum Cartridge Catheter (intravascular catheter)List Number: 100G8920610H1ARTG Number: 161905
  • Manufacturer

Manufacturer

  • 제조사 모회사 (2017)
  • Source
    DHTGA