Equipment for paclitaxel with air intake, model AMC9627, hazard class II, Brand name: Baxter, Record number: 10068390316. Number of lots: 14H04V366, 14I01T752 and 14K28T473. 의 안전성 경고

Agência Nacional de Vigilância Sanitária (ANVISA)에 따르면, 해당 안전성 경고 는 Brazil 에서 Baxter Hospitalar Ltda.; Baxter Limited. 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
  • 사례 ID
    1776
  • 날짜
    2015-12-21
  • 사례 국가
  • 사례 출처
    ANVISA
  • 사례 출처 URL
  • 비고 / 경고
    Brazilian data is current through June 2018. All of the data comes from Anvisa, 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 Brazil.
  • 데이터 추가 비고
    Baxter informs that this kind of leak can be easily detected during the priming of the equipment or in the initial set up that is performed with a solution, even without the drug. However, if not checked immediately, the leak could have adverse consequences to the patient's health by generating a break in the sterility of the fluid pathway with subsequent contamination of the solution, which was considered serious and would potentially require medical intervention; or by possible contact of the solution with the skin, which could cause irritation. Since this type of leak is easily detected, the risk of medically reversible or transient damage in the general population is considered remote and in a high-risk population of fatal adverse events is also considered remote.
  • 원인
    Leakage in the air intake of the equipment to paclitaxel.
  • 조치
    Collection and destruction of products. Action code FCA 2015-089. The company guides customers: 1. Check in your inventory if you own the lots that will be collected; 2. Immediately cease the use of lots of this product; 3. Complete Annex 1 - Customer Response Form contained in the letter to the customer and then send it to Baxter. 4. Forward a copy of this Urgent Product Pickup letter to other departments or institutions according to their procedures. In the case of a distributor / reseller who has distributed this product to other establishments, please advise your customers about this Urgent Product Pickup by forwarding the communication letter to everyone.

Manufacturer