Device Recall LIMA Modular Revision Hip Stem 의 리콜

U.S. Food and Drug Administration에 따르면, 해당 리콜 는 United States 에서 Encore Medical, Lp 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
    76209
  • 사례 위험등급
    Class 2
  • 사례 연번
    Z-1191-2017
  • 사례 시작날짜
    2017-01-10
  • 사례 출판 날짜
    2017-02-11
  • 사례 상황
    Terminated
  • 사례 국가
  • 사례 종료 날짜
    2017-03-31
  • 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
    Prosthesis, hip, semi-constrained (metal uncemented acetabular component) - Product Code KWA
  • 원인
    Lima proximal bodies were inadvertently re-sterilized. the safety screw which affixes the distal and proximal bodies of the stem includes a thread-locking plug made from uhmwpe, which is not approved for repeated gamma sterilization.
  • 조치
    DJO Global sent an Urgent Field Safety Notice letter dated January 10, 2017 to customers. The letter identified the affected product, problem and actions to be taken. Customers were asked to complete the Acknowledgement and receipt Form. Customers were instructed to contact Customer Service at 1-800-456-8696 to explore options for a replacement order.

Device

  • 모델명 / 제조번호(시리얼번호)
    1005528A, 1006882A, 1107305A, 1101798A, 1100565A, 1005531A, 1211716A, 1007408A, 1004038B, 1005533D, 1106805A, 1203471A, 1005533C, 1100565A, 1101795A, 1007079A, 1005532A, 1100560A
  • 의료기기 분류등급
  • 의료기기 등급
    3
  • 이식된 장치?
    Yes
  • 유통
    US Nationwide - US Nationwide in the states of MS, OH, RI, NY, OK, TX, CA, HI
  • 제품 설명
    LIMA Modular Revision Hip Stem Model 428-01-050_110 || Product Usage: || The Modular Revision Femoral hip stem is made up of a modular stem coupled with a proper neck by means of a Morse taper stabilized during the implantation phase by a safety screw. This system is particularly indicated for revision surgery on both uncemented and cemented femoral implants, when there is significant bone loss and an abnormal meta-epiphyseal anatomy of the femur.
  • Manufacturer

Manufacturer

  • 제조사 주소
    Encore Medical, Lp, 9800 Metric Blvd, Austin TX 78758-5445
  • 제조사 모회사 (2017)
  • Source
    USFDA