5.5 mm arthroscopic burs from Stryker 의 리콜

L’Agence nationale de sécurité du médicament et des produits de santé (ANSM)에 따르면, 해당 리콜 는 France 에서 STRYKER 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
  • 날짜
    2005-03-02
  • 사례 국가
  • 사례 출처
    ANSM
  • 사례 출처 URL
  • 비고 / 경고
    French data is current through early September 2018. All of the data comes from L’Agence nationale de sécurité du médicament et des produits de santé (ANSM), 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 France.
  • 데이터 추가 비고
  • 조치
    Afssaps was informed by STRYKER of the withdrawal of the market on February 21, 2005 from the references and batches specified in the attached message, the medical device called "5.5 mm arthroscopic cutters" following reports of patient burns due to overheating resulting from the combination of 3 conditions (oversize inner sleeve of the burs, applying excessive force and not activating the suction function, contrary to the instructions for use). No incident has been reported in France. The company Stryker directly notified the recipients of the lots concerned with the attached message (21/02/2005) (109 KB). The relevant European Competent Authorities have informed by the manufacturer of this measure.

Device

  • 모델명 / 제조번호(시리얼번호)
  • 제품 설명
    medical_device
  • Manufacturer

Manufacturer

  • 제조사 모회사 (2017)
  • Source
    LAANSM