TD-Synergy Blood Bank module connected to TD-Synergy (known as LIS connection) 의 안전성 경고

Department of Health에 따르면, 해당 안전성 경고 는 Hong Kong 에서 TECHNIDATA SAS 에 의해 제조된 제품과 관련되어 있습니다.

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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
    2013-04-19
  • 사례 출판 날짜
    2013-04-19
  • 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: technidata td-synergy blood bank module connected to td-synergy (known as lis connection) medical device manufacturer, technidata sas, has issued a field safety notice concerning a defect affecting all versions of the td-synergy blood bank module connected to td-synergy (known as lis connection). the blood bank module retains one of the two blood group determinations whereas it should not retain any and should alert the users. this issue identified at the montfort site (canada) occurs when the two blood group determinations are received in the same astm message. the td-synergy blood bank module version is v04.71.B, but this defect could potentially occur in all versions. the identified scenario is the following: for a patient with no known blood group on the blood bank module, when an astm message is received from td-synergy including two different blood group determinations, the blood bank module retains one of the determinations as the blood group for this patient whereas it should not retain any and should alert the users. this defect can occur if the following conditions are met: blood bank module connected to td-synergy (lis connection) unknown blood group on the blood bank module two different blood group determinations for the same sample in the first transmission of the astm file blood bank module is set with extended compatibility (see general settings parameter) specific dongle option « double determination on a single sample » the severity is considered very high as the defect could lead to an incorrect transfusion. the probability is assessed as low given the number of conditions to meet. the manufacturer advises users to find correction packages corresponding to the td-synergy blood bank module on the technidata website and contact their support team if the corresponding correction package is not available on the website. according to the manufacturer, the affected products were distributed in hong kong. if you are in possession of the affected products, please contact your supplier for necessary actions. posted on 19 april 2013.

Device

  • 모델명 / 제조번호(시리얼번호)
  • 제품 설명
    Medical Device Safety Alert: TECHNIDATA TD-Synergy Blood Bank module connected to TD-Synergy (known as LIS connection)
  • Manufacturer

Manufacturer