V240040029 cable 의 리콜

U.S. Food and Drug Administration에 따르면, 해당 리콜 는 United States 에서 Flight Medical Ltd. 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
    59827
  • 사례 위험등급
    Class 1
  • 사례 연번
    Z-1041-2012
  • 사례 시작날짜
    2011-08-10
  • 사례 출판 날짜
    2012-02-21
  • 사례 상황
    Terminated
  • 사례 국가
  • 사례 종료 날짜
    2012-05-21
  • 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
    Ventilator, continuous, facility use - Product Code CBK
  • 원인
    The recall was initiated because flight medical innovations ltd. has identified a problem may occur when contact between an exposed unused wire and the grounding wire occurs. if this contact occurs the ventilator may reset and switch off.
  • 조치
    Newport Medical Instruments, Inc., the U.S. distributor for Flight Medical Ltd., sent a letter dated August 23, 2011 to all affected customers. The letter describes the product, problem, and actions to be taken by the customers. The letter instructs customers to immediately discontinue use of the affected product. An Acknowledgement Form was attached to the letter for customers to complete and return via fax at (714) 427-0489 or e-mail to Regulatory@NewportMedical.com. Replacement product will be provided once the form is received. Contact Newport Medical's Technical Service Group at 800-451-3111 ext. 500 for questions regarding this notice. Updated: The firm posted a press release on 02/12/12 Isreal time, notifying customers of update regarding its voluntary recall of remote alarm cable, part number V24-00400-29, used to connect a Newport HT50 mechanical ventilator to a nurse station. The press release notified: The recalled cable may negatively affect Newport HT50 ventilators manufactured prior to 2007. Affected units may shutdown unexpectedly. The FDA has classified this action as a Class I recall. On August 23, 2011, Flight Medical sent an urgent Recall Notice to affected customers through its distributor, Newport Medical Instruments, Inc. (Newport Medical), to stop using the alarm cable immediately and to contact Newport Medical in order to receive an upgraded version of the cable. In the notification letter, the customers were notified of the affected cables and that an upgraded version of the cable would be provided to them free of charge. Customers, including Newport Medical are requested to dispose of the affected cables properly. Instructions to customers: Customer inquiries related to this action should be addressed to Newports Technical Service Group at (800) 4513111, extension 500.

Device

  • 모델명 / 제조번호(시리얼번호)
    P/N V24-00400-90 Rev. B
  • 의료기기 분류등급
  • 의료기기 등급
    2
  • 이식된 장치?
    No
  • 유통
    Nationwide Distribution.
  • 제품 설명
    V24-00400-29 cable, an accessory to the Newport HT50 ventilator. || The V24-00400-29 cable is an accessory to the Newport HT50 ventilator intended to transfer the alarm signal from the ventilator to a nurse remote station.
  • Manufacturer

Manufacturer

  • 제조사 주소
    Flight Medical Ltd., 13 Hamelacha Street, Lod Israel
  • Source
    USFDA