Spectra Optia Apheresis System 의 안전성 경고

Department of Health에 따르면, 해당 안전성 경고 는 Hong Kong 에서 Terumo BCT 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
    2014-07-21
  • 사례 출판 날짜
    2014-07-21
  • 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 bct spectra optia apheresis system medical device manufacturer, terumo bct, has issued a field safety notice (fsn) concerning spectra optia apheresis system. all serial numbers are affected. the manufacturer is recalling the sensor because a small number of these components have failed either disrupting or prematurely ending an ongoing apheresis procedure. the manufacturer has investigated all reported return line air detector (rlad) failures and identified the following failure modes: electrostatic discharge (esd) during manufacturing or installation can damage the rlad component, eventually resulting in failure of the component. when this occurs, the spectra optia system is placed in a safe state and cannot be used until it is serviced. esd protective measures were implemented to resolve this issue. during a procedure, air can be falsely detected in the return line when the plastic tubing decouples (slightly moves away) from the sensor. when this occurs, an “air detected in the return line” alarm is generated by the system. after completing an air recovery procedure, the apheresis procedure can sometimes be continued by confirming there is no air in the return line and verifying that the return pump tubing makes good contact with the rlad sensor. however, if sequential air recoveries are required, the system may terminate the procedure. the procedure must then be re-initiated with a new tubing set. the manufacturer has modified the rlad sensor to eliminate this “decoupling” and the resulting false rlad alarm. according to the manufacturer, the primary risk to health occurs during mononuclear and granulocyte cell collection procedures, where patients/donors receive a mobilizing agent (e.G., g-csf) prior to the cellular collection. should an rlad failure result in the premature termination of a cell collection procedure, an additional procedure and administration of g-csf could be required. the manufacturer advises users of the followings: continue to use spectra optia system. if users experience “air detected in the return line” alarms that users cannot clear, and users do not see air in the return line, they should call the terumo bct support center. specialists will review the alarms and coordinate repair of the device, if needed. the manufacturer has modified the rlad sensor. based on extensive laboratory testing and field validation data, the manufacturer expects the modified component to reduce the occurrence of false air detections due to tubing decoupling. the manufacturer will replace the existing rlad sensor with the redesigned component. 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 21 july 2014.

Device

  • 모델명 / 제조번호(시리얼번호)
  • 제품 설명
    Medical Device Safety Alert: Terumo BCT Spectra Optia Apheresis Systems
  • Manufacturer

Manufacturer