Device Recall Churchill Medical Systems, Inc. DRESSING CHANGE KIT 의 리콜

U.S. Food and Drug Administration에 따르면, 해당 리콜 는 United States 에서 Vygon Corporation 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
    61945
  • 사례 위험등급
    Class 2
  • 사례 연번
    Z-1807-2012
  • 사례 시작날짜
    2012-05-11
  • 사례 출판 날짜
    2012-06-13
  • 사례 상황
    Terminated
  • 사례 국가
  • 사례 종료 날짜
    2013-03-11
  • 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
    Heparin, vascular access flush - Product Code NZW
  • 원인
    Manufacturer issued a voluntary recall on multiple lots of vy(tm)flush heparin lock flush syringes therefore vygon has subsequently initiated a recall on vygon branded heparin lock flush syringes and kits containing the syringes.
  • 조치
    VYCON sent an URGENT MEDICAL DEVICE RECALL letter dated May 10, 2012, to all affected customers. The firm expanded their recall on May 25, 2012 by sending a second letter with additional lots and products. The letter identified the product, the problem, and the action to be taken by the customer. Customers were instructed to check their inventory and quarantine any affected product. Customers should contact Vycon's Customer Service Department at 1-800-473-5414 for a Return Merchandise Authorization number. Customers were instructed to enter the number on the space provided on the Recall Acknowledgment and Inventory Return Form, sign and date form and fax to Vycon at 215-672-6740. Customers should return the affected product as well as the original signed Recall Acknowledgment and Inventory Form using the instructions from Customer Service involving product pick-up. All inventory will be credited. If product was further distributed the Urgent Medical Device Recall letter should be provided to their customers. For questions regarding this recall call 215-672-6740.

Device

  • 모델명 / 제조번호(시리얼번호)
    Product Code AMS-7091CP - lot 11C119.
  • 의료기기 분류등급
  • 의료기기 등급
    2
  • 이식된 장치?
    No
  • 유통
    Nationwide Distribution including AZ, CA, DE, FL, IL, IN, IA, KS, KY, MD, MA, MI, MN, MO, NJ, NY, OH, PA, UT, VA, WA, WV, and WI.
  • 제품 설명
    Churchill Medical Systems, Inc. DRESSING CHANGE KIT || Prefilled syringes included in the kit are used to maintain the patency of indwelling catheter lumens
  • Manufacturer

Manufacturer