Medline Latex Free Vaginal Delivery CDSLF 의 리콜

U.S. Food and Drug Administration에 따르면, 해당 리콜 는 United States 에서 Medline Industries 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
    49107
  • 사례 위험등급
    Class 2
  • 사례 연번
    Z-0016-2009
  • 사례 시작날짜
    2008-08-04
  • 사례 출판 날짜
    2008-10-10
  • 사례 상황
    Terminated
  • 사례 국가
  • 사례 종료 날짜
    2008-10-20
  • 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
    Cesarean Section Kit - Product Code OHM
  • 원인
    The latex free labor & delivery packs contain a latex nuk pacifier. the pacifier is packaged separately and offers no risk of exposure of latex particles to other components of the pack.
  • 조치
    Recall letters dated 8/4/08 were sent to the direct accounts on the same date, informing them that the labor and delivery packs were labeled Latex Free, but contained a Latex Nuk pacifier. The letters were customized for each account, listing the specific affected reorder numbers and lot numbers shipped to each account. The accounts were requested to immediately check their stocks for the affected lot numbers and quarantine the affected product found. The accounts were given three options: A) Attach the enclosed stickers to the packs so that the user is aware of the latex Nuk pacifier, B) Call Medline to receive replacement non-latex pacifiers, but also place the stickers on the packs, C) Return the packs to Medline for replacements. The accounts were requested to complete the enclosed response form, indicating which option the account selected and whether they needed any additional stickers, and fax the form back to Medline at 847-643-4482 by 8/18/08. Any questions were directed to Kathy Dunne at 1-866-359-1704.

Device

  • 모델명 / 제조번호(시리얼번호)
    VAGINAL DELIVERY CDS-LF reorder #CDS830006A, lots 05CD1909, 05ED0962, 05FD1796; reorder #CDS830014I, lots 06KD2998, 07AD2164, 07CD0437, 07ED0711, 07FD2205, 07GD3892, 07ID1876, 07ID2031;  reorder #CDS830014K, lots 07LD3284, 08DD0454, 08DD2313, 08FD1231, 08FD3833;  reorder #CDS830161B, lots 06JG0627, 06KG0324, 06KG0769, 06LG0181, 07BG0190, 07EG1256, 07FG0454, 07FG0684, 07FG0686, 07IG1497, 07LG191, 08AG2182, 08DG0043, 08FG1527, 06ED2094, 06FD0326, 06HD0006;
  • 의료기기 분류등급
  • 의료기기 등급
    2
  • 이식된 장치?
    No
  • 유통
    Nationwide Distribution --- including states of Alabama, Arizona, Georgia, Missouri, Nevada, New Jersey, and Washington.
  • 제품 설명
    Medline Latex Free Vaginal Delivery CDS-LF; a single patient prescription procedure pack and disposables, including a Gerber Nuk Pacifier; Made in USA by Medline Industries, Inc., Mundelein, IL 60060
  • Manufacturer

Manufacturer

  • 제조사 주소
    Medline Industries Inc, 1 Medline Pl, Mundelein IL 60060-4486
  • Source
    USFDA