G4 PLATINUM Replacement Receiver Kit 의 안전성 경고

Department of Health에 따르면, 해당 안전성 경고 는 Hong Kong 에서 Dexcom Inc 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
    2012-11-27
  • 사례 출판 날짜
    2012-11-27
  • 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: dexcom g4 platinum replacement receiver kit the medicines and healthcare products regulatory agency (mhra), united kingdom has posted a field safety notice concerning g4 platinum replacement receiver kit (model no.: str-gl-001) manufactured by dexcom inc. the affected products can be identified by the following serial numbers: sm23470992, sm23471039, sm23471062, sm23471144, sm23471148. the affected lot number is 5045847. dexcom g4 platinum replacement receiver kits (str-gl-001, lot 5045847) sent to advanced therapeutics united kingdom are not affixed with a ce mark and are not approved for distribution within the european economic area (eea). five units were shipped from dexcom's manufacturing site in san diego, ca, usa to advanced therapeutics, uk on 24 october 2012. the subject devices accept and display glucose measurements in mg/dl, whereas devices approved for use in the uk must display glucose measurement in mmol/l. this product nonconformance has no effect on safety and/or patient health. there are no reports of illness or injury associated with this issue. there is no hazard involved as the receivers in the kits use mg/dl as the unit of measure for blood glucose rather than mmol/l. the device requires entry of blood glucose readings from a blood glucose meter for calibration and start up prior to use. the subject devices will not accept the mmol/l blood glucose meter measurement ranges, and would not be able to calibrate at start-up, eliminating the potential for false values to be displayed. in addition, the end user is extremely likely to notice the incorrect unit of measure for blood glucose prior to an attempt to use the device. the manufacturer advises that further distribution or use of any remaining product affected by this recall should cease immediately. all affected products must be quarantined and returned to the manufacturer. for details, please refer to the mhra website: http://www.Mhra.Gov.Uk/safetyinformation/safetywarningsalertsandrecalls/ fieldsafetynotices/con205394 if you are in possession of the affected product, please contact your supplier for necessary actions. posted on 27 november 2012.

Device

  • 모델명 / 제조번호(시리얼번호)
  • 제품 설명
    Medical Device Safety Alert: Dexcom G4 PLATINUM Replacement Receiver Kit
  • Manufacturer

Manufacturer