Events

Device Recall Shiley TracheoSoft 의 리콜

U.S. Food and Drug Administration에 따르면, 해당 리콜 는 United States 에서 Nellcor Puritan Bennett 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
    29653
  • 사례 위험등급
    Class 1
  • 사례 연번
    Z-1312-04
  • 사례 시작날짜
    2004-07-08
  • 사례 출판 날짜
    2004-08-07
  • 사례 상황
    Terminated
  • 사례 국가
    United States
  • 사례 종료 날짜
    2005-11-29
  • 사례 출처
    USFDA
  • 사례 출처 URL
    https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfres/res.cfm?id=34291
  • 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 and the Product Classification were added by ICIJ.
    The parent company information is based on 2017 public records. The device classification information comes from FDA’s Product Classification by Review Panel data.
  • 데이터 추가 비고
    unknown device name - Product Code ---
  • 원인
    Device component can become disconnected or dislodged, leading to ineffective ventilation, which could result in serious injury or death.
  • 조치
    On 7/8/04, the firm initiated the recall. ***[After CDRH recommendations for class I recall situation, the firm issued PR via AP on 8/6/04.]*** .

Device

Device Recall Shiley TracheoSoft
  • 모델명 / 제조번호(시리얼번호)
    All units of these models.
  • 의료기기 분류등급
    Anesthesiology Devices
  • 유통
    The tracheostomy tubes were distributed to 4,179 direct US and US Territory customers. The firm has also distributed products to Canada, the UK, Latin America and Japan. The firm's branches in those countries are handling the recall activities in those countries. The firm manufactured 95,923 units and distributed 71.021 throughout the US and US territories. 4,481 are on hold at the Nellcor distribution facility, and approximately 3000 units are currently in distribution.
  • 제품 설명
    Shiley TracheoSoft¿ XLT Extended Length Tracheostomy tube; || Model Numbers: || 72110-050, size 5, Proximal Extension, Uncuffed; || 72110-060, size 6, Proximal Extension, Uncuffed; || 72110-070, size 7, Proximal Extension, Uncuffed; || 72110-080, size 8, Proximal Extension, Uncuffed; || 72120-050, size 5, Promixal Extension, Cuffed; || 72120-060, size 6, Promixal Extension, Cuffed; || 72120-070, size 7, Promixal Extension, Cuffed; || 72120-080, size 8, Promixal Extension, Cuffed; || 73110-050, size 5, Distal Extension, Uncuffed; || 73110-060, size 6, Distal Extension, Uncuffed; || 72110-070, size 7, Distal Extension, Uncuffed; || 73110-080, size 8, Distal Extension, Uncuffed; || 73120-050, size 5, Distal Extension, Cuffed; || 73120-060, size 6, Distal Extension, Cuffed; || 73120-070, size 7, Distal Extension, Cuffed; || 73120-080, size 8, Distal Extension, Cuffed; || 77100-050, size 5 XLT Disposal Inner Cannula; || 77100-060, size 6 XLT Disposal Inner Cannula; || 77100-070, size 7 XLT Disposal Inner Cannula; || 77100-080, size 8 XLT Disposal Inner Cannula || Manufactured by Mallinckrodt Medical, County Westmeath Cornamaddy, Athlone, Ireland; || Customer Service: Mallinckrodt, Inc. St Louis, MO 63134
  • Manufacturer
    Nellcor Puritan Bennett

Manufacturer

Nellcor Puritan Bennett
  • 제조사 주소
    Nellcor Puritan Bennett, 4280 Hacienda Dr, Pleasanton CA 94588-2719
  • Source
    USFDA