Nonvented Y-Set 의 안전성 경고

Department of Health에 따르면, 해당 안전성 경고 는 Hong Kong 에서 Hospira 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
    2014-04-17
  • 사례 출판 날짜
    2014-04-17
  • 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.
    ICU Medical, Inc. acquired from Pfizer in early 2017, Hospira Infusion Systems, the portion of Hospira dedicated to develop infusion pumps.
  • 데이터 추가 비고
    Medical Device Safety Alert
  • 원인
    Medical device safety alert: hospira nonvented y-set medical device manufacturer, hospira, has issued a medical device safety alert concerning its nonvented y-set for transurethral resection (list number: 06543-01). the impacted batches are 13106ns, 13170ns, 13251ns, 14261ns, 14262ns, 15139ns, 16117ns, 17131ns, 17132ns, 17184ns, 18110ns, 18111ns, 18182ns, 19133ns, 20122ns, 20123ns, 20124ns, 20205ns, 22146ns, 22147ns, 22148ns, 22149ns, 23103ns, 23104ns, 23105ns, 23106ns, 24156ns, 25130ns, 25131ns, 27109ns, 27253ns, 27286ns, 28136ns, 28137ns, 29094ns, 29095ns, 29096ns, 30194ns, 30195ns, 30196ns, 31042ns, 31043ns, 32229ns, 32230ns, 33138ns, 33139ns, 33140ns, 34286ns and 35117ns. in the complaint review, the manufacturer has discovered the issue of incomplete sealing in the secondary package of the affected batches of devices. the issue occurred either because the sterile pack was not sealed properly or the tyvek cover sheet was not centered on the bottom tray of the pack, allowing openings at the edge of the sterile package. the open packaging of the affected product may lead to loss of product sterility, delay in initiating therapy, introduction of infectious agent and particulate onto the surface of the irrigation set. up to date, the manufacturer did not receive any complaint or adverse reporting associated with the incomplete sealing of the package. the manufacturer advises affected users not to use the package if it is not intact. 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 17 april 2014.

Device

  • 모델명 / 제조번호(시리얼번호)
  • 제품 설명
    Medical Device Safety Alert: Hospira Nonvented Y-Set
  • Manufacturer

Manufacturer

  • 제조사 모회사 (2017)
  • Source
    DH