Device Recall GemStar 의 리콜

U.S. Food and Drug Administration에 따르면, 해당 리콜 는 United States 에서 Hospira 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
    68200
  • 사례 위험등급
    Class 2
  • 사례 연번
    Z-2031-2014
  • 사례 시작날짜
    2014-01-31
  • 사례 출판 날짜
    2014-07-10
  • 사례 상황
    Terminated
  • 사례 국가
  • 사례 종료 날짜
    2016-08-30
  • 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.
    ICU Medical, Inc. acquired from Pfizer in early 2017, Hospira Infusion Systems, the portion of Hospira dedicated to develop infusion pumps.
  • 데이터 추가 비고
    Pump, infusion - Product Code FRN
  • 원인
    The connection between the beeper subassembly and the pump may fail. the gemstar infusion pump will identify this failure during the "self-test" while powering up which will result in a beeper error ("code 10/001/000"). this beeper error (code 10/001/000) is a service alarm that places the pump in an inoperable mode and requires service before it can be returned to service.
  • 조치
    Hospira sent an URGENT MEDICAL DEVICE RECALL letter dated January 31, 2014 was sent to all affected customers. The letter included instructions for customers to: 1) inform potential users of these devices of the notification, 2) if the beeper error occurs during power up, remove the device from service immediately, 3) report any beeper errors to Hospira by calling 800-441-4100 (Monday - Friday, 8:00 AM - 5:00 PM CST) or e-mail ProductComplaintsPP@hospira.com, 4) complete the attached reply form and return it to the fax number of e-mail address on the form (even if there is no product in inventory), and 5) if the products were further distributed, notify those customers that received the products and ask them to contact Stericycle at 855-827-6578 (Monday - Friday, 8:00 AM - 5:00 PM EST) to receive a reply form. A subsequent letter was sent on February 18, 2014 that included a correction to the description of the error code generated when a beeper wire failure occurs. That letter included identical instructions as those found in the January 31, 2014 letter for recipients to follow.

Device

  • 모델명 / 제조번호(시리얼번호)
  • 의료기기 분류등급
  • 의료기기 등급
    2
  • 이식된 장치?
    No
  • 유통
    Worldwide Distribution - US: Nationwide in the state of AK, AL, AR, AZ, CA, CO, CT, DE, FL, GA, HI, IA, ID, IL, IN, KS, KY, LA, MA, MD, ME, MI, MN, MO, MS, MT, NC, ND, NE, NH, NJ, NM, NV, NY, OH, OK, OR, PA, RI, SC, SD, TN, TX, UT, VA, VT, WA, WI, WV, WY including District Of Columbia, Guam, Puerto Rico; and the countries of Austria, Australia, Bahrain, Belgium, Canada, Chile, France, Germany, Greece, Guatemala, Hong Kong, Italy, Jordan, Kuwait, Lebanon, Libya, Luxembourg, Malaysia, Mexico, Netherlands, Oman, Portugal, Saudi Arabia, Slovenia, South Africa, Spain, Switzerland, Taiwan, Thailand, Turkey, United Arab Emirates, United Kingdom, Venezuela
  • 제품 설명
    GemStar infusion pump, List numbers 13000 and 13100, GemStar Infusion Pump (pain management) List number 13150. Used for intravenous, arterial, subcutaneous, short-term epidural infusion and parenteral administration of general I.V. fluids, medications, nutritional fluids, and blood/blood products.
  • Manufacturer

Manufacturer

  • 제조사 주소
    Hospira Inc., 275 N Field Dr, Lake Forest IL 60045-2579
  • 제조사 모회사 (2017)
  • Source
    USFDA