Events

Device Recall Reprocessed Ethicon Xcel Trocar Sleeve 의 리콜

U.S. Food and Drug Administration에 따르면, 해당 리콜 는 United States 에서 Stryker Sustainability Solutions 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
    71805
  • 사례 위험등급
    Class 2
  • 사례 연번
    Z-2468-2015
  • 사례 시작날짜
    2015-07-10
  • 사례 출판 날짜
    2015-08-27
  • 사례 상황
    Terminated
  • 사례 국가
    United States
  • 사례 종료 날짜
    2015-12-04
  • 사례 출처
    USFDA
  • 사례 출처 URL
    https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfres/res.cfm?id=139129
  • 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
    Laparoscope, general & plastic surgery, reprocessed - Product Code NLM
  • 원인
    Stryker sustainability solutions has received reports indicating that devices from one lot (lot# 3574704) were labeled as 100mm models (cb5lt) while the devices inside of the packaging were 75mm models (cb5st).
  • 조치
    On 07/10/15 the firm sent out notification letters to all customers. The letter states for the customer to discontinue use of the affected lot, and to use other trocar lots reporcessed by the firm. The firm requests that the Recall Effectiveness Check Form be completed. The firm is going to be sending a sales representative to the facilities to check inventory for the affected trocars. A Recall Effectiveness Check will also be completed. If the form indicates that affected devices remain in inventory a prepaid shipping label will be issued for the return of the product. Customers will receive credit for all affected devices returned. The form must be completed even if no affected devices are found in inventory. Stryker Sustainability Solutions Complaint Hotline: 1-888-888-3433 x5555

Device

Device Recall Reprocessed Ethicon Xcel Trocar Sleeve
  • 모델명 / 제조번호(시리얼번호)
    Lot number 3574704 UDI Code: (01)00885825014421(17)180310(10)3574704 Model Number: CB5ST (labeled as CB5LT)
  • 의료기기 분류등급
    Gastroenterology-Urology Devices
  • 의료기기 등급
    2
  • 이식된 장치?
    No
  • 유통
    U.S. Nationwide Distribution to the following states of:: NV, NM, TX, and MI.
  • 제품 설명
    Stryker || Sustainability Solutions || CB5LT || Ethicon Endo-Surgery, Inc. || Excel Trocar Sleeve || w/Stability Sleeve || 5mm x 100mm || Reprocessed by Stryker Sustainability Solutions || Product Usage: || The Reprocessed Ethicon ENDOPATH¿ XCEL Universal Trocar Stability Sleeve is a sterile single patient use device with a radiolucent sleeve. The trocar sleeve contains two seals that accommodate instruments 5mm in diameter. Together, these two seals minimize gas leakage when instruments are inserted or withdrawn through the trocar. A stopcock valve is compatible with standard luer lock fitting and provides attachment for gas insufflation and desufflation. The stopcock is in the closed position when it is parallel to the sleeve.
  • Manufacturer
    Stryker Sustainability Solutions

Manufacturer

Stryker Sustainability Solutions
  • 제조사 주소
    Stryker Sustainability Solutions, 1810 W Drake Dr, Tempe AZ 85283-4327
  • 제조사 모회사 (2017)
    Stryker
  • Source
    USFDA