Alaris Infusion pump administration sets 의 리콜

Department of Health, Therapeutic Goods Administration에 따르면, 해당 리콜 는 Australia 에서 CareFusion Australia 316 Pty Ltd 에 의해 제조된 제품과 관련되어 있습니다.

이것은 무엇인가요?

의료기기에 문제가 생겼을 경우 제조사가 이를 바로잡거나 시장에서 회수하는 조치를 말한다. 회수(Recall)는 의료기기에 결함이 있거나, 건강에 위협이 되거나, 또는 결함도 있고 건강에도 위협이 될 경우에 발생한다.

데이터에 대해 더 자세히 알아보기 여기
  • 사례 유형
    Recall
  • 사례 ID
    RC-2018-RN-00722-1
  • 사례 위험등급
    Class II
  • 사례 시작날짜
    2018-06-19
  • 사례 국가
  • 사례 출처
    DHTGA
  • 사례 출처 URL
  • 비고 / 경고
    Australian data is current through July 2018. All of the data comes from the Australian Therapeutic Goods Administration, 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 recall data from the U.S. and Australia.
  • 데이터 추가 비고
  • 원인
    The bd alaris infusion pump administration sets require priming prior to use as described in the directions for use (dfu). bd has identified a potential issue with the bd alaris infusion pump administration sets manufactured during january 2017 through march 2018. the issue pertains to the back check valve and the ability to prime the administration sets. the manufacturer has determined the root causes leading to this issue are associated with: 1. excessive solvent used to connect the tubing to the back check valve leading to an obstruction of the fluid path, thus preventing the priming of the set. 2. a higher “cracking” pressure of the back check valve.To date, no injuries have been reported as a result of this issue.
  • 조치
    CareFusion is advising that users can continue to use the product. When a set cannot be appropriately primed, users may be able to increase the pressure by gently squeezing the IV bag following these steps: 1. If no drops are observed, gently squeeze the bag at the fluid level with one hand once. Observe if set is able to prime. 2. If no drops are observed repeat this up to 3 times. 3. If this method is not effective discard and replace the administration set. 4. Consider having additional administration sets available in clinical areas where high risk infusions are administered.

Device

  • 모델명 / 제조번호(시리얼번호)
    Alaris Infusion pump administration sets Product Codes: 2120-0500 , 2420-0007 , 2420-0500, 10015489, 11426965 ARTG Number:125916
  • Manufacturer

Manufacturer