Events

Device Recall Bivona TTS Cuffed Pediatric Tracheostomy Tube 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
    60449
  • 사례 위험등급
    Class 1
  • 사례 연번
    Z-0667-2012
  • 사례 시작날짜
    2011-11-28
  • 사례 출판 날짜
    2012-01-19
  • 사례 상황
    Terminated
  • 사례 국가
    United States
  • 사례 종료 날짜
    2014-10-17
  • 사례 출처
    USFDA
  • 사례 출처 URL
    https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfres/res.cfm?id=106117
  • 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, tracheostomy (w/wo connector) - Product Code BTO
  • 원인
    Difficulty disconnecting accessories from the bivona uncuffed neonatal, pediatric and flextend tracheostomy tubes tr3 connector, which may result in a delay in initiating therapy or patient discomfort. if excessive force is used to detach the accessory, this may result in decannulation of the tube which could result in serious injury or death; especially if no replacement tracheostomy tube is imm.
  • 조치
    Smith Medical sent an Urgent Field Safety Notice dated November 28, 2011, via U.S. Mail to all affected consignees. The notice identified the product, description of problem, and actions to be taken. This notice included a Customer Information Bulletin and Urgent Field Safety Notice Confirmation Form. Customers were instructed to 1) identify all affected unused product in inventory and segregate it to a quarantine location; 2) complete and return the attached Confirmation Form by fax to 219-989-7259 or email to bivona.tr3@smiths-medical.com; and 3) distributors were instructed to stop distributing and provide Smith Medical with a list of their customers, including contact details, so that Smith Medical can notify the customers of this notice. For questions contact Smiths Medical Customer Service at 800-258-5361, Option 1.

Device

Device Recall Bivona TTS Cuffed Pediatric Tracheostomy Tube
  • 모델명 / 제조번호(시리얼번호)
    Lot numbers: 1692762, 1754787, 1793510, 1817480, 1883552, 1679945, 1692763, 1692764, 1796683, 1793511, 1814096, 1835048, 1848177, 1887782, 1887781, 1631521, 1648147, 1655832, 1671969, 1663886, 1737254, 1725345, 1774655, 1787342, 1825908, 1883553, 1914924, 1692765, 1704648, 1713955, 1729057, 1749590, 1754789, 1804373, 1821991, 1851439, 1856221, 1878010, 1896190, 1913143, 1631522, 1648152, 1683683, 1713956, 1729101, 1848175, 1848176, 1868263, 1875208, 1883555, 1908926, 1919157, 1663878, 1671970, 1687752, 1692766, 1696953, 1708840, 1774656, 1787343, 1793512, 1821992, 1875209, 1868264, 1923407, 1666284, 1683684, 1701033, 1713957, 1749591, 1864913, 1856222, 1883554, 1887783, 1896191, and 1900043.  Reorder numbers: 67SP025, 67SP030, 67SP035, 67SP040, 67SP045, 67SP050, and 67SP055.
  • 의료기기 분류등급
    Anesthesiology Devices
  • 의료기기 등급
    2
  • 이식된 장치?
    No
  • 유통
    Worldwide Distribution - USA Nationwide: AZ, CA, CO, CT,DE, FL, GA, HI, IL, IN, KS, KY, LA, SC, TX, OR, NJ, MO, UT, MI, NY, NM, MA, MN, MS, NC, ND, NE, NH, NV, OH, OK, OR, RI, SD, TN, VA, VT, WA, WI, WV including Washinton DC, Australia, Austria, Barbados, Belgium, Brazil, Canada, Chile, Cyprus, Czech Republic, Denmark, Egypt, Finland, France, Germany, Gibraltar, Great Britain (UK), Greece, Hong Kong, Ireland, Israel, Italy, Kuwait, Libya, Malaysia, Netherlands, New Zeland, Norway, Poland, Portugal, Qatar, Russian Federation, Saudi Arabia, Singapore, Spain, Sweden, Switzerland, United Arab Emirates, United States, Vatican City State
  • 제품 설명
    Bivona TTS Cuffed Pediatric Tracheostomy Tube || Sizes 2.5 - 5.5 (With a Straight Neck Flange) || Product Usage: This tube is intended to provide direct airway access for a tracheostomized patient for up to 29 days. It may be reprocessed up to 5 times for single patient reuse.
  • Manufacturer
    Smiths Medical ASD, Inc.

Manufacturer

Smiths Medical ASD, Inc.
  • 제조사 주소
    Smiths Medical ASD, Inc., 5700 W 23rd Ave, Gary IN 46406-2617
  • 제조사 모회사 (2017)
    Smiths Group Plc
  • Source
    USFDA