Events

Device Recall Portex Endotracheal Tube Holders 의 리콜

U.S. Food and Drug Administration에 따르면, 해당 리콜 는 United States 에서 Smiths Medical ASD, 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
    68739
  • 사례 위험등급
    Class 1
  • 사례 연번
    Z-2539-2014
  • 사례 시작날짜
    2014-07-07
  • 사례 출판 날짜
    2014-08-28
  • 사례 상황
    Open, Classified
  • 사례 국가
    United States
  • 사례 출처
    USFDA
  • 사례 출처 URL
    https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfres/res.cfm?id=128847
  • 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
    Tube, tracheal (w/wo connector) - Product Code BTR
  • 원인
    The tube fastener on the et tube holder may compress the tracheal tube when used which may cause difficulty when locking the et tube holder in place or difficulty when passing a suction catheter.
  • 조치
    Smiths Medical sent an Urgent Medical Device Recall Notice dated July 11, 2014, to all affected customers. The letter informed customers of the recall and instructed them to inspect their inventory and segregate any unused affected products and to complete and return the Recall Confirmation Form, by Fax 1-800-621-2590 or email to endotrachealtubeholders@smiths-medical.com. Customers with questions were instructed to call Smiths Medical's Customer Service Department at 1-800-258-5361. For questions regarading this recall call 866-216-8806.

Device

Device Recall Portex Endotracheal Tube Holders
  • 모델명 / 제조번호(시리얼번호)
    Lot Numbers: 2481849, 2474643, 2470640, 2470639, 2465819, 2462292, 2462291, 2457748, 2453455, 2448671, 2443372, 2438612, 2428206, 2420088, 2412135, 2394046, 2394045, 2394044, 2385648, 2380341, 2376618, 2376489, 2365439,  2361588, 2343298, 2329576, 2326894, 2322814, 2317088, 2309465, 2309464, 2298739, 2298738, 2286586, 2278062, 2271339, 2188449, 2179222, 2164289, 2146292, 2142175, 2137959, 2128629, 2119945, 2109011, 2099501, 2090215,  2068121, 2063971, 2063970, 2042408, 12046, 11871, 11862, 11858, 11696, 11693, 11656, 11653
  • 의료기기 분류등급
    Anesthesiology Devices
  • 의료기기 등급
    2
  • 이식된 장치?
    No
  • 유통
    Worldwide Distribution - USA including AK, AR, AZ, CA, CO, CT, DC, FL, GA, IA, IL, IN, KS, KY, LA, MA, MD, MI, MN, MO, MS, MT, NC, NE, NH, NJ, NM, NY, OH, OK, OR, PA, SC, SD, TN, TX, UT, VA, WA, WI, WV and Internationally to CA, CY, GB, IE, IT, JE, KW, MT, PL, RU, SA, ZA.
  • 제품 설명
    H4002S Neonatal/Paed.Intubation Kit 3.0mm Murphy, 15mm Conn, Holder || Pediatric Endotracheal Intubation Kit
  • Manufacturer
    Smiths Medical ASD, Inc.

Manufacturer

Smiths Medical ASD, Inc.
  • 제조사 주소
    Smiths Medical ASD, Inc., 10 Bowman Dr, Keene NH 03431-5043
  • 제조사 모회사 (2017)
    Smiths Group Plc
  • Source
    USFDA