Radiometer ABL90Flex analysers running V3.1MR1 or below 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-2014-RN-01365-1
  • 사례 위험등급
    Class I
  • 사례 시작날짜
    2014-12-24
  • 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
    Radiometer has recently become aware of a potential significant clinical issue with patient results if the inlet is left open after aspiration of the patient sample for more than 30 seconds. if the inlet is accidentally left open after processing a patient sample the abl90 analyser sounds a warning bell, places a warning message on the screen and also initiates a voice message continuously repeating “please close the inlet”the problem can occur after the following sequence of actions:1. the operator aspirates patient sample a and forgets to close the inlet 2. the inlet is left open for more than 30 seconds before it is closed3. an operator aspirates patient sample bin this case the results for patient sample b are affected by this issue.Radiometer is currently developing a mechanism to be included in a future software upgrade to eliminate the possibility of this error. a label to be attached to the machine is provided to re-inforce the correct instructions for use.
  • 조치
    Operators are reminded of the requirement to close the inlet when prompted by the analyser, as per the labelling and the Operator Manual. In the event the inlet is left open by mistake, a series of corrective steps is provided to customers as an interim measure. A warning label is also provided to customers to attach to the machine to re-inforce the correct instructions for use. Customers are advised that a look back over previous results may be required at the discretion of the Medical Director Radiometer is currently developing a mechanism to be included in a future software upgrade that will eliminate the possibility of this error. This action has been closed-out on 20/04/2017.

Device

  • 모델명 / 제조번호(시리얼번호)
    Radiometer ABL90Flex analysers running V3.1MR1 or belowARTG Number: 228382An in vitro diagnostic medical device (IVD)
  • Manufacturer

Manufacturer