MagNA Pure 96 Instrument 의 안전성 경고

Department of Health에 따르면, 해당 안전성 경고 는 Hong Kong 에서 Roche Diagnostics 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
    2014-03-05
  • 사례 출판 날짜
    2014-03-05
  • 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: roche magna pure 96 instrument medical device manufacturer, roche diagnostics has issued a medical device safety alert concerning magna pure 96 instrument. the following devices are affected: material number 06541089001 (ivd labelled), serial number 4065 material number 05195322001 (lsr labelled), serial number 1115 there is a potential for sample mismatch when magna pure 96 xml order files are transmitted from any upstream instrument (including but not limited to hamilton magna starlet instrument) or any user developed“file sharing”order input to magna pure 96 instruments using magna pure software version 2.0.3 and earlier. with this current xml anomaly, the automated workflow is potentially impacted. the orders transferred from upstream instruments and/or an lis displayed in the magna pure 96 orders screen can be out of sequence, which can lead to mismatched sample information. the manufacturer explains that the magna pure 96 software assumes a one to one correlation between the “number” field specified in the xml file and the sample information and its actual sample position on the plate. automation partners who create xml file transmissions to be sent to the magna pure 96 instrument may not realize that the “number” field must be directly tied to the actual position in the plate, as this requirement is not explicitly stated in the magna pure host interface manual. if this is not followed, sample mismatches may occur when data is imported into the magna pure 96 software, without generating any error message or notification. if the xml interface functionality to downstream instruments is also utilized, then mismatched sample information would be passed on to the instruments where the samples are analyzed leading to results being assigned to the wrong samples. the magna pure 96 system host interface manual and software will be updated to address this issue. as an interim measure, customers using a magna starlet are advised to review the magna pure 96 orders tab and confirm that the correct sample order is associated with the appropriate corresponding plate well position before starting a run. customers using a lab developed system are advised to ensure that the orders are transmitted sequentially with no gaps. according to the local supplier, the affected products were distributed to hong kong. if you are in possession of the affected products, please contact your supplier for necessary actions. postedposted on 05 march 2014.

Device

  • 모델명 / 제조번호(시리얼번호)
  • 제품 설명
    Medical Device Safety Alert: Roche MagNA Pure 96 Instrument
  • Manufacturer

Manufacturer