PLUM LifeCare 5000 Series and PLUM XL Families of Infusers 의 안전성 경고

Department of Health에 따르면, 해당 안전성 경고 는 Hong Kong 에서 Hospira 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
    2013-12-12
  • 사례 출판 날짜
    2013-12-13
  • 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: hospiraplum lifecare 5000 series and plum xl families of infusers the australia therapeutic goods administration (tga) posted a medical device safety alert concerning plum lifecare 5000 series and plum xl families of infusers manufactured by hospira inc.The affected products are identified as follows:- plum lifecare 5000, list number: 02507 plum xl, list number :11555 plum xlm, list number: 11846 plum xld, list number: 11859 the door roller assembly on the plum a lifecare 5000 series and plum xl has the potential to break which can lead to possible unrestricted flow and/or over delivery during the removal of the iv administration set's cassette from the pump. the manufacturer is requesting hospitals to take the following steps to inspect the door assemble prior to loading the cassette: open the cassette door by pulling on the lever; unlatch the cassette door by pushing on the door release tab and pulling the door down; visually inspect the door roller pin for any evidence of the damage or door roller misalignment; and ensure that the door roller spins smoothly with a finger touch. if any door rollers or pins appear loose, broken or missing, hospira advises users to remove the device from use. the manufacturer is in the process of retiring the plum lifecare 5000 and plum xl in 2015. for details, please visit the following tga website:http://www.Tga.Gov.Au/sara/arn-detail.Aspx?k=rc-2013-rn-01288-1 if you are in possession of the affected product, please contact your supplier for necessary actions. posted on 13 december 2013.

Device

  • 모델명 / 제조번호(시리얼번호)
  • 제품 설명
    Medical Device Safety Alert: HospiraPLUM LifeCare 5000 Series and PLUM XL Families of Infusers
  • Manufacturer

Manufacturer

  • 제조사 모회사 (2017)
  • Source
    DH