STERIS Harmony LL 500/700 Surgical Light 의 리콜

U.S. Food and Drug Administration에 따르면, 해당 리콜 는 United States 에서 Steris Corp 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
    53475
  • 사례 위험등급
    Class 2
  • 사례 연번
    Z-0414-2010
  • 사례 시작날짜
    2009-09-11
  • 사례 출판 날짜
    2009-11-23
  • 사례 상황
    Terminated
  • 사례 국가
  • 사례 종료 날짜
    2012-03-01
  • 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
    Surgical Lamp - Product Code FTD
  • 원인
    Dr¿ger medical ag & co., kgaa informed steris corporation that they received (4) reported international cases where a welded seam at the joint of the spring-loaded arm of the dr¿ger sola 500/700 surgical light broke as a result of a crack that had slowly developed over time. the steris harmony ll 500/700 surgical light is a private label version of the dr¿ger sola 500/700 surgical light.
  • 조치
    The firm sent Urgent Product Correction letters, dated Sept. 11, 2009, to their customers. The letter identified the problem and stated that Drager had supplied STERIS the replacement spring arms and that a STERIS Service Technician would perform the replacement. The letter also stated that the correction would be performed at no charge to the customers. According to the letter, customers would be contacted by their STERIS Service Representative to arrange a convenient time for replacement of potentially affected spring arms. In the meantime, the letter states that customers should use their surgical lights in accordance with the guidelines presented in the Operator's Manual. Questions or concerns regarding the letter should be directed to Barbara Rich at 440-392-7318 or your local STERIS account manager.

Device

  • 모델명 / 제조번호(시리얼번호)
    Part Number: YG18568; Serial Numbers: Year 2002 - 0111 072 XXXXX to 0111 122 XXXXX; Year 2003-0111 013 XXXXX to 0111 123 XXXXX; Year 2004-0111 014 XXXXX to 0111 124 XXXXX; Year 2005-0111 015 XXXXX to 0111 125 XXXXX; and Year 2006-0111 016 XXXXX to 0111 066 XXXXX - (XXXXX means every 5-digit serial number).
  • 의료기기 분류등급
  • 의료기기 등급
    2
  • 이식된 장치?
    No
  • 유통
    Worldwide Distribution -- USA, including the states of AL, AR, CA, CO, CT, FL, GA, HI, IL, IN, KS, LA, MA, MN, MO, MS, NC, NH, NJ, NV, NY, OH, PA, RI, SC, TN, TX, UT, VA, WA, WI & WY and the country of Canada.
  • 제품 설명
    STERIS Harmony LL 500/700 Surgical Light, Vertical Spring-Loaded Arm. || Intended for local illumination of the operating and examination area of the patient in treatment rooms.
  • Manufacturer

Manufacturer

  • 제조사 주소
    Steris Corp, 5960 Heisley Rd, Mentor OH 44060
  • Source
    USFDA