COBE Spectra Bone Marrow Processing Set 의 안전성 경고

Department of Health에 따르면, 해당 안전성 경고 는 Hong Kong 에서 Terumo BCT Inc. 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
    2013-10-16
  • 사례 출판 날짜
    2013-10-16
  • 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: terumo cobe spectra bone marrow processing set medical device manufacturer, terumo bct inc., has issued a field safety notice concerning cobe spectra bone marrow processing tubing set. the affected catalogue number is 70630, and the affected lot numbers are 10t15261, 10t15296, 12t15257, 05u15258 and 09u15271. the lot numbers 10t15261 and 10t15296 have an expiration date of 1 oct 2013. a leak at the tubing bond to the y-connector in the bone marrow processing (bmp) set can, with very low probability, resulting in bacterial contamination of a transfusion product. terumo bct is aware of four reported events related to a leak at the tubing bond to the y-connector in the bmp set that did not result in adverse event and does not consider this failure mode a systemic issue. if the contaminated product is not tested prior to transfusion, patients may experience serious infections and other related serious adverse events. the manufacturer advises users not to use the affected products. it has implemented corrective actions to improve the manufacturing process for bonding the y-connector to the tubing. for example, 100% inspection was added to the manufacturing operating procedure to verify bonding specifications for the bond to the bone marrow bag. according to the local supplier, the affected products were distributed in hong kong. if you are in possession of the products, please contact your supplier for necessary actions. posted on 16 october 2013.

Device

  • 모델명 / 제조번호(시리얼번호)
  • 제품 설명
    Medical Device Safety Alert: Terumo COBE Spectra Bone Marrow Processing Set
  • Manufacturer

Manufacturer