LifePort¿, Dual Lumen Profile Plastic Dual Port with Poly Urethane Catheter Kit, Product Code/REF: LPS 7255 의 리콜

U.S. Food and Drug Administration에 따르면, 해당 리콜 는 United States 에서 Horizon Medical Products 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
    30048
  • 사례 위험등급
    Class 2
  • 사례 연번
    Z-0256-05
  • 사례 시작날짜
    2004-09-20
  • 사례 출판 날짜
    2004-11-24
  • 사례 상황
    Terminated
  • 사례 국가
  • 사례 종료 날짜
    2005-03-01
  • 사례 출처
    USFDA
  • 사례 출처 URL
  • 비고 / 경고
    U.S. data is current through June 2018. All of the data comes from the U.S. Food and Drug Administration, except for the category Manufacturer Parent Company.
    The Parent Company was added by ICIJ.
    The parent company information is based on 2017 public records.
  • 데이터 추가 비고
    Port & Catheter, Implanted, Subcutaneous, Intravascular - Product Code LJT
  • 원인
    The product has an incorrectly sized introducer included in the kit. the kit contains a 12 french introducer instead of a 7 french introducer.
  • 조치
    Consignees were notified by letter on 09/20/2004.

Device

  • 모델명 / 제조번호(시리얼번호)
    Catalog #LPS 7255, Lot #20474
  • 의료기기 분류등급
  • 의료기기 등급
    2
  • 이식된 장치?
    Yes
  • 유통
    FL, GA, LA, MD, NJ, OK, TX, VA
  • 제품 설명
    LifePort¿, Dual Lumen Profile Plastic Dual Port with Poly Urethane Catheter Kit, Product Code/REF: LPS 7255, Manufactured by: Horizon Medical Products, Inc., One Horizon Way, P.O. Box 627, Manchester, GA 31816.The devices are placed in a molded PVC tray. The tray is sealed with a Tyvek lid. The inner sealed tray is then placed in another tray, the Instruments for Use (IFU), Patient Information Booklet (PIB), patient ID card and its label, the IFU for the locking mechanism and the labeling describing the materials and priming volume, are all placed on top of that lid before sealing the outer tray with another Tyvek lid. The product label is applied to the outer tray lid and the entire package-tray inside a tray ¿ is then sterilized. The primary sterile barrier is the inner sealed tray.
  • Manufacturer

Manufacturer

  • 제조사 주소
    Horizon Medical Products Inc, 1 Horizon Way, Manchester GA 31816-1749
  • Source
    USFDA