Autopen, Autopen 24, Densupen and Autopen 3ml for Teriparatide 의 안전성 경고

Department of Health에 따르면, 해당 안전성 경고 는 Hong Kong 에서 Owen Mumford Ltd 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
    2014-12-16
  • 사례 출판 날짜
    2014-12-16
  • 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: owen mumford autopen, autopen 24, densupen and autopen 3ml for teriparatide the medicines and healthcare products regulatory agency (mhra), united kingdom posted a medical device safety alert concerning autopen classic, autopen 24, densupen and autopen 3ml for teriparatide manufactured by owen mumford ltd. the affected product codes are an3800, an3810, an4200, an4210, an1281 and an1251. according to the manufacturer, a proportion of devices from the lot codes listed in the field safety notice have a potential mechanical fault. the fault presents itself in the following ways: a) a dose may be dialled-up but the dose selector will not hold that dose and instead will spin straight back to zero. b) the dose may be dialled-up and the dose selector will hold the dose momentarily, but will then spin back to zero. this potential risks to patient are: a) the patient will not be able to use the pen, no dose can be delivered. b) the patient may only receive a partial dose and will not know how much insulin has been delivered. the affected products are being recalled. for details, please refer to the following link: http://www.Mhra.Gov.Uk/safetyinformation/safetywarningsalertsandrecalls/fieldsafetynotices/con484997 if you are in possession of the affected products, please contact your supplier for necessary actions. posted on 16 december 2014.

Device

  • 모델명 / 제조번호(시리얼번호)
  • 제품 설명
    Medical Device Safety Alert: Owen Mumford Autopen, Autopen 24, Densupen and Autopen 3ml for Teriparatide
  • Manufacturer

Manufacturer