NeuraGen Nerve Guide and NeuraWrap Nerve Protector 의 안전성 경고

Department of Health에 따르면, 해당 안전성 경고 는 Hong Kong 에서 Integra LifeScience Corporation 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
    2013-04-24
  • 사례 출판 날짜
    2013-04-24
  • 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: integra neuragen nerve guide and neurawrap nerve protector the australia therapeutic goods administration (tga) has issued a medical device safety alert concerning neuragen nerve guide and neurawrap nerve protector manufactured by integra lifescience corporation. the affected catalogue numbers are png130, png320, png520, png620, nw320, nw520 and the affected lot numbers are 1112378, 1112106, 1112004, 1112030, 1111938, 1112038. through an internal quality assurance review of processes, the manufacturer found that the production process may have deviated during the manufacture of specific lots of product. the product lots in question passed all product finished goods testing, are sterile, and were tested and accepted for endotoxin levels. however, due to the process deviation they may have been released with higher levels of endotoxins than permitted by the specifications for the products. integra is recalling the affected products and advises the clinicians to monitor their patients in the postoperative period in accordance with standard hospital or clinician protocol. for details, please visit the following tga website: http://www.Tga.Gov.Au/sara/arn-detail.Aspx?k=rc-2013-rn-00353-1 if you are in possession of the affected products, please contact your supplier for necessary actions. posted on 24 april 2013.

Device

  • 모델명 / 제조번호(시리얼번호)
  • 제품 설명
    Medical Device Safety Alert: Integra NeuraGen Nerve Guide and NeuraWrap Nerve Protector
  • Manufacturer

Manufacturer