Device Recall Coseal Surgical Sealant 의 리콜

U.S. Food and Drug Administration에 따르면, 해당 리콜 는 United States 에서 Baxter Bioscience 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
    55825
  • 사례 위험등급
    Class 2
  • 사례 연번
    Z-1949-2010
  • 사례 시작날짜
    2010-01-14
  • 사례 출판 날짜
    2010-07-02
  • 사례 상황
    Terminated
  • 사례 국가
  • 사례 종료 날짜
    2010-12-22
  • 사례 출처
    USFDA
  • 사례 출처 URL
  • 비고 / 경고
    U.S. data is current through June 2018. All of the data comes from the U.S. Food and Drug Administration, except for the category Manufacturer Parent Company.
    The Parent Company was added by ICIJ.
    The parent company information is based on 2017 public records.
  • 데이터 추가 비고
    Polymerizing Sealant - Product Code NBE
  • 원인
    The recall is being conducted as a precautionary measure due to out of specification results at the 18 month and 21 month time points (out of the 24 month licensed shelf life to expiration) for the percent thiol substitution during a coseal stability study. the parameter that is out of specification is an indicator of possible failure for the product to gel appropriately.
  • 조치
    The recall notification was initiated on January 14, 2010 with the firm sending a Product Recall letter and attached Customer Reply Form to the affected consignees. The recall letter informed the consignees of the reason for recall and requested them to immediately stop the usage/distribution of the lots noted above and to quarantine any units you may still have in your inventory. The letter provided instruction for product return. The letter also requested the consignees to please forward the recall information as appropriate to other services/facilities/departments that they may have provided this product to. Consignees were instructed to complete the Customer Reply Form, and fax it as soon as possible to 888-345-4261. Consignees with questions were instructed to contact Stericycle at 877-870-4486.

Device

  • 모델명 / 제조번호(시리얼번호)
    Lot Numbers: HA080942, HA080943, HA081001E, HA081046E, HA081102, HA081132, HA081235, HA090139, HA090241, & HA090342.
  • 의료기기 분류등급
  • 의료기기 등급
    3
  • 이식된 장치?
    Yes
  • 유통
    Nationwide Distribution
  • 제품 설명
    Coseal Surgical Sealant 4mL, Product Codes: 934071 & 934074. || Indicated for use in vascular reconstructions to achieve adjunctive hemostasis.
  • Manufacturer

Manufacturer

  • 제조사 주소
    Baxter Bioscience, 1 Baxter Way, Westlake Village CA 91362-3811
  • 제조사 모회사 (2017)
  • Source
    USFDA