Stryker TRIO/TRIO 의 리콜

U.S. Food and Drug Administration에 따르면, 해당 리콜 는 United States 에서 Stryker Spine 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
    62663
  • 사례 위험등급
    Class 2
  • 사례 연번
    Z-2235-2012
  • 사례 시작날짜
    2012-04-25
  • 사례 출판 날짜
    2012-08-22
  • 사례 상황
    Terminated
  • 사례 국가
  • 사례 종료 날짜
    2013-02-27
  • 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
    Orthosis, spinal pedicle fixation - Product Code MNI
  • 원인
    The front cover of instructions for use (ifu) #noli135b03rev02 was improperly marked with a "sterile" logo in the lower right corner. the products these ifus were packed with are sold as "non-sterile" and require sterilization before use in surgery.
  • 조치
    Stryker sent an "URGENT MEDICAL DEVICE RECALL NOTIFICATION" letter to affected customers. The letter identifies the product, problem, and actions to be taken by the customers. A Customer Response Form was attached for customers to complete and return via fax to 201-760-8370. Contact the firm at 201-760-8298 for questions regarding this notice.

Device

  • 모델명 / 제조번호(시리얼번호)
    Code information listed in the following format: Manufacturer Part Number/Prodcut Description/Corresponding IFU Part Number/Affected Lot #s are as follows:  48900445/Trio Standard Post Screw 5.5x55mm/#NOLI135B03Rev02/57281 and 57201  48900450/Trio Standard Post Screw 5.5x60mm/#NOLI135B03Rev02/57197   48900455/Trio Standard Post Screw 4.5x45mm/#NOLI135B03Rev02/57198  48900555/Trio Standard Post Screw 4.5x50mm/#NOLI135B03Rev02/56599  48900560/Trio Standard Post Screw 4.5x55mm/#NOLI135B03Rev02/57192
  • 의료기기 분류등급
  • 의료기기 등급
    2
  • 이식된 장치?
    Yes
  • 유통
    Distributed in Atlanta, Georgia.
  • 제품 설명
    The Instructions For Use for the following: || Stryker TRIO+ 4.5 x 45 mm STANDARD POST SCREW || Stryker TRIO+ 4.5 x 50 mm STANDARD POST SCREW || Stryker TRIO+ 4.5 x 55 mm STANDARD POST SCREW || Stryker TRIO+ 5.5 x 45 mm STANDARD POST SCREW || Stryker TRIO+ 5.5 x 60 mm STANDARD POST SCREW || Manufactured by: STRYKER Spine SAS, Z.I. Marticot - 33610 - Cestas-France +33 (0)5.57.97.06.30 http://www.stryker.com || Distributed in the USA by: Stryker Spine, 2 Pearl Ct., Allendale, NJ 07401-1677 USA +1-201-750-8000. || The system is intended for posterior, non-cervical pedicle and non-pedicle pedicle fixation of the spine. It is indicated for: degenerative disc disease (DDD), spondylolisthesis, fracture, dislocation, spinal stenosis, scoliosis kyphosis, lordosis, spinal tumor, pseudarthrosis, and failed previous fusion.
  • Manufacturer

Manufacturer

  • 제조사 주소
    Stryker Spine, 2 Pearl Ct, Allendale NJ 07401-1611
  • 제조사 모회사 (2017)
  • Source
    USFDA