immunochemistry modules e170, cobas e 601 and cobas e 602 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
    2017-07-06
  • 사례 출판 날짜
    2017-07-06
  • 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 diagnostics immunochemistry modules e170, cobas e 601 and cobas e 602 medical device manufacturer, roche diagnostics, has issued a medical device safety alert concerning its immunochemistry modules e170 (catalogue number: 04998642001), cobas e 601 (catalogue number: 04745922001) and cobas e 602 (catalogue number: 05990378001). the systems affected are modular analytics evo, cobas 6000 analyzer series and cobas 8000 modular analyzer series. the manufacturer is informing customers that a sample mismatch may occur in the immunochemistry modules (cobas e 602, cobas e 601 and e170 modules) due to a software limitation. the sample mismatch is only occurs if the following conditions are simultaneously met (i.E. very rare occurrence): immunochemistry module (cobas e 602, cobas e 601 and e170 modules) is included in its respective system (cobas 8000 modular analyzer series, cobas 6000 analyzer series, modular analytics, modular analytics evo) the “module rack buffer setting” ≠”1” → two or more sample racks stay in the idling/processing line (l-line) consecutively during operation. one rack (rack a) is undergoing sampling and the following rack (rack b) is waiting for measurement. the gripper (t/v carrier) fails to pick up the last vessel (cup) on rack a. as a consequence, the measurement for the sample in the last vessel which failed to be picked up is canceled and the warning "tip/cup pick up error” (caution level) is issued. sample position 1 of the following rack (rack b) is empty or has no test order for the immunochemistry module. according to the manufacturer, the root cause has been identified and a newly software version fixing that issue will be released by nov 2017. meanwhile and until the new software version is available, the local supplier will contact the user and change the setting for the “module rack buffer setting” to 1. when the new software version is available it will be installed as a mandatory update to the system. the manufacturer advises users to use the interim solution of the field safety notice until the local supplier changes the setting for the “module rack buffer setting” to 1 according to the local supplier, the affected products, except modular analytics evo , are distributed in hong kong. if you are in possession of the affected products, please contact your supplier for necessary actions. posted on 6 july 2017.

Device

  • 모델명 / 제조번호(시리얼번호)
  • 제품 설명
    Medical Device Safety Alert: Roche Diagnostics immunochemistry modules E170, cobas e 601 and cobas e 602
  • Manufacturer

Manufacturer