Medfusion Syringe Pump Model Series 3500 and 4000 의 안전성 경고

Department of Health에 따르면, 해당 안전성 경고 는 Hong Kong 에서 Smiths Medical 에 의해 제조된 제품과 관련되어 있습니다.

이것은 무엇인가요?

안전성 경고는 의료기기 제품과 관련된 중요한 정보와 권고사항을 담고 있습니다. 물론 안전성 경고가 배포되었다고 해서 해당 제품이 무조건 안전하지 않은 제품이라는 것은 아닙니다. 보건의료업계 종사자와 의료기기 사용자들에게 배포되는 안전성 경고에는 회수(recall)도 포함될 수 있습니다. 제조사가 안전성 경고를 작성하기도 하지만, 보건당국에서 작성하는 경우도 있습니다.

데이터에 대해 더 자세히 알아보기 여기
  • 사례 유형
    Safety alert
  • 날짜
    2017-08-02
  • 사례 출판 날짜
    2017-08-02
  • 사례 국가
  • 사례 출처
    DH
  • 사례 출처 URL
  • 비고 / 경고
    Hong Kong data is current through September 2018. All of the data comes from the Department of Health (Hong Kong), except for the categories Manufacturer Parent Company and Product Classification.
    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, based on matches of data from the U.S. and Hong Kong.
  • 데이터 추가 비고
    Medical Device Safety Alert
  • 원인
    Medical device safety alert: smiths medical medfusion syringe pump model series 3500 and 4000 the medicines and healthcare products regulatory agency (mhra) of the united kingdom has posted a medical device safety alert concerning medfusion syringe pump model series 3500 and 4000, manufactured by smiths medical. the manufacturer became aware that the thread lock material used on a fastening screw can be ineffective. as a result, the medfusion pump syringe barrel clamp mechanism may loosen and decrease the pump’s ability to accurately detect the outside diameter measurement of the syringe barrel, causing an “invalid syringe size” alarm to occur. a delay in the initiation of an infusion or an interruption of an active infusion has the potential to result in serious injury or death. the effect to the patient would depend on the patient’s condition, the therapy involved, and the amount of time the therapy would be delayed or interrupted. the “invalid syringe size” alarm triggered as a result of this potential issue alerts healthcare practitioners to the problem. although no serious injuries or deaths have been reported as a result of this issue, the manufacturer recommends against using the affected devices until repair work is completed. the users are instructed to locate the affected devices, which would be repaired by the manufacturer. for details, please refer to the mhra’s website: https://www.Gov.Uk/drug-device-alerts/field-safety-notice-24-to-28-july-2017 if you are in possession of the affected products, please contact your supplier for necessary actions. posted on 2 august 2017.

Device

  • 모델명 / 제조번호(시리얼번호)
  • 제품 설명
    Medical Device Safety Alert: Smiths Medical Medfusion Syringe Pump Model Series 3500 and 4000
  • Manufacturer

Manufacturer