Suture Washer 의 리콜

U.S. Food and Drug Administration에 따르면, 해당 리콜 는 United States 에서 Arthrex, Inc. 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
    75050
  • 사례 위험등급
    Class 3
  • 사례 연번
    Z-2918-2016
  • 사례 시작날짜
    2016-08-12
  • 사례 상황
    Open, Classified
  • 사례 국가
  • 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
    Washer, bolt nut - Product Code HTN
  • 원인
    The device was assembled incorrectly. suture and washer were not assembled; components were placed loose in the package.
  • 조치
    Consignees were notified 8/12/2016 of the potentially affected devices; Product/Batch Numbers: AR-7000-818T Batch #10028617. For Healthcare Professionals: immediately discontinue use of all affected products with stated numbers in their possession. Call (855) 552-5056 or email returns@arthrex.com with the product number, lot, and quantities so they may ship replacement products and expedite return of recalled product. To please complete the "Recall Acknowledgement of Receipt: postal card and return to Arthrex, Inc. Distributing Agencies: Immediately identify and hold all stated products in your inventory. Call 888-519-7255 ext. 72067 or e-mail AIM@arthrex.com Attn: Christi Zimmer. Have product number, lot number and quantities you may have so replacement product may be shipped and expedite the return of the recalled product. Please complete the "Recall Acknowledgement of Receipt" postal card and return to Arthrex. Inc. Any questions about the return of products to call 866-267-9138 and ask for Ellen Barry. Also by email to complaints@arthrez.com.

Device

  • 모델명 / 제조번호(시리얼번호)
    Unique Device Identifier (UDI): 00888867118607;  Catalog # AR-7000-18T; Batch #10028617.
  • 의료기기 분류등급
  • 의료기기 등급
    2
  • 이식된 장치?
    Yes
  • 유통
    OR, NY, MN, KY, CA, ID, CO, MA, and FL. Thailand.
  • 제품 설명
    Arthrex Suture Washer
  • Manufacturer

Manufacturer

  • 제조사 주소
    Arthrex, Inc., 1370 Creekside Blvd, Naples FL 34108-1945
  • 제조사 모회사 (2017)
  • Source
    USFDA