Peritoneal Dialysis Transfer Set 의 안전성 경고

Department of Health에 따르면, 해당 안전성 경고 는 Hong Kong 에서 Baxter Healthcare Ltd. 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
    2013-03-05
  • 사례 출판 날짜
    2013-03-05
  • 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: baxter peritoneal dialysis transfer set medical device manufacturer,baxter healthcare ltd., has issued a letter to customers concerning capd solution transfer set with locking connector(product code 5c4160)and minicap extended life pd transfer set with twist clamp (product code 5c4482). baxter would like to provide an important information regarding changes that are being made to instructions for use(ifu) for baxter peritoneal dialysis transfer set with the above product codes to improve product labeling and ensure consistency of information across the baxter transfer set product family.Key additions to the ifu include: the set is to be used with the baxter locking titanium adapter for peritoneal dialysis catheter in disconnect applications and in cycler applications where aseptic connections and disconnections are performed at the transfer set/cycler set juncture. wipe for a minimum of 1 minute around the connection between the titanium adapter and the transfer set or locking cap with a sterile gauze pad soaked in povidone-iodine. it is recommended that thyroid function be monitored in patients with small peritoneal dialysate fill volumes, typically infants and children. reuse or reprocessing of a single use device may lead to contamination and compromised device function or structural integrity. do not use if tip protectors are not in place. this product does not contain natural rubber latex. baxter advises customers to communicate to the patient forapplicable changes to the ifu and emphasize the importance of following the ifu at each pd transfer set installation or exchange. according to the local supplier, the affected products were distributed in hong kong. if you are in possession of the affected product, please contact your supplier for necessary actions. posted on 5 march 2013.

Device

  • 모델명 / 제조번호(시리얼번호)
  • 제품 설명
    Medical Device Safety Alert: Baxter Peritoneal Dialysis Transfer Set
  • Manufacturer

Manufacturer