Bard ConQuest PTA Balloon Dilatation Catheter (Intended for use in Percutaneous Transluminal Angioplasty of the femoral, renal and iliac arteries) 의 리콜

Department of Health, Therapeutic Goods Administration에 따르면, 해당 리콜 는 Australia 에서 Bard 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-2015-RN-00286-1
  • 사례 위험등급
    Class I
  • 사례 시작날짜
    2015-03-27
  • 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.
  • 데이터 추가 비고
  • 원인
    Bard peripheral vascular (bpv) has identified that the product code / lot number combinations affected may be at risk of having deflation related issues.In the event a pta balloon will not deflate, immediate intervention is required in order to deflate the balloon and allow for continued blood flow. in many cases, this can be accomplished percutaneously by inserting a device (i.E., guidewire or sheath) to the pta balloon and puncturing the balloon and/or a sheath, allowing its withdrawal. this can usually be completed through the same vascular access, however, may require additional access. in the event a pta balloon cannot be deflated while in the extremities (i.E., superficial femoral artery or av fistula), it may be possible to insert a sterile needle through the skin and reach the balloon and pierce it in order to deflate it. in the event a percutaneous approach cannot successfully deflate the pta balloon, an open surgical approach will be required.
  • 조치
    Customers are advised to remove any affected product from their shelves and contact Bard Australia Customer Service to arrange for any affected product to be returned and replaced. This action has been closed-out on 1/06/2016.

Device

  • 모델명 / 제조번호(시리얼번호)
    Bard ConQuest PTA Balloon Dilatation Catheter (Intended for use in Percutaneous Transluminal Angioplasty of the femoral, renal and iliac arteries)Product Codes: CQ75124, CQ75124, CQ75124, CQ75124, CQ75124, CQ75124, CQ75124, CQ75124, CQ75124Lot Numbers:REYA0973, REYA2566, REYC0372, REYC0950, REYC1426, REYC2200, REYC2365, REYC2825, REYC2575ARTG Number: 137802
  • 의료기기 분류등급
  • Manufacturer

Manufacturer