HemoCue Glucose 201 RT Microcuvettes (used with HemoCue Glucose 201 RT and HemoCue Glucose 201 RT DM analysers). An in vitro diagnostic medical device (IVD) 의 리콜

Department of Health, Therapeutic Goods Administration에 따르면, 해당 리콜 는 Australia 에서 Radiometer Pacific Pty 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
    RC-2016-RN-00237-1
  • 사례 위험등급
    Class II
  • 사례 시작날짜
    2016-03-09
  • 사례 국가
  • 사례 출처
    DHTGA
  • 사례 출처 URL
  • 비고 / 경고
    Australian data is current through July 2018. All of the data comes from the Australian Therapeutic Goods Administration, 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 recall data from the U.S. and Australia.
  • 데이터 추가 비고
  • 원인
    Hemocue has recently become aware of a production related problem that affects hemocue glucose 201rt microcuvettes. during an internal investigation a minor deviation was found, which may cause the microcuvettes to not perform as intended. there was an incorrect position for the sleigh in the final punch which affects the grouping of cuvettes with respect to measuring level. the accuracy of glucose levels below 4.1mmol/l may deviate by up to +0.9 mmol/l, resulting in falsely high results. there is also a low possibility that results in the range of 6.6-8.8 mmol/l may be falsely elevated.No harm to patients has been reported. however, there is a risk that a false high result for low glucose levels could lead to delayed or missed diagnosis of hypoglycaemia, as clinical symptoms are not always present.
  • 조치
    Radiometer is advising users that the affected product can continue to be used in adults. The affected lots should not be used in neonates or infants. Users should verify low or marginal results via another method.

Device

  • 모델명 / 제조번호(시리얼번호)
    HemoCue Glucose 201 RT Microcuvettes (used with HemoCue Glucose 201 RT and HemoCue Glucose 201 RT DM analysers). An in vitro diagnostic medical device (IVD)Product Code: 114701Batch Numbers: 1506998, 1507909, 1508920, 1405990, 1407901, 1410921, 1411931, 1501939, 1501950, 1504972, 1506995 ARTG Number: 222660
  • Manufacturer

Manufacturer