Device Recall EliA Sample Diluent, Article number, 83102301 의 리콜

U.S. Food and Drug Administration에 따르면, 해당 리콜 는 United States 에서 Phadia US 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
    76343
  • 사례 위험등급
    Class 2
  • 사례 연번
    Z-1253-2017
  • 사례 시작날짜
    2017-01-30
  • 사례 출판 날짜
    2017-02-24
  • 사례 상황
    Terminated
  • 사례 국가
  • 사례 종료 날짜
    2017-08-07
  • 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
    Antibodies, anti-cyclic citrullinated peptide (ccp) - Product Code NHX
  • 원인
    Erroneous elia test results related to problems with liquid level detection and diluent pipetting in phadia 250 instruments, and deformed bottles. investigation showed problems with the liquid level detection in diluent bottle batch jjca resulting in aspiration of no or too low volumes of liquid from the diluent bottle and from the dilution plate.
  • 조치
    Phadia AB, part of Thermo Fisher Scientific, is voluntarily recalling EliA Sample Diluent, Article number, 83-1023-01, lots JM3Y, JS0B, JP87, JK5N, and JU9C, written notices were mailed via FedEx on 01/30/2017. There have been reports of instrument malfunctions for Phadia 250 due to deformed bottles for the below mentioned product and lots. The deformation of the bottle can cause an erroneous volume detection by the instrument which will result in insufficient aspiration of sample diluent, thus generating insufficient dilution of patient samples. The deformation is described as a flange or brim, located on the inside lower part of the vial opening. ACTIONS TO BE TAKEN BY THE CUSTOMER/USER: ¿ Stop using the affected lots of the above mentioned product lots ¿ Please, return or attest to scrapping of any unused product lots to the manufacturer and order replacement products free of charge. ¿ Review your records to determine if you have had instrument problems due to deformed bottles. If you find the instrument error message 3-145 RIGHT ARM LIQUID DETECTION BELOW LOWER LIMIT Target 2, please collect all log files available and/or contact customer support, who will further assist in assessing possible impact on the test results in scope. ¿ Fill in the Medical Device Recall return response on page 3 and return to the manufacturer by e-mail. If customers have any questions, please contact Phadia US, Inc. at 1-800-346- 4364, option #2.

Device

  • 모델명 / 제조번호(시리얼번호)
    EliA Sample Diluent, Article number, 83-1023-01, lots JM3Y, JS0B, JP87, JK5N, and JU9C
  • 의료기기 분류등급
  • 의료기기 등급
    2
  • 이식된 장치?
    No
  • 유통
    Domestic: AR, CA, CO, FL, GA, IL, IN, KY, LA, MI, MN, MO, MT, NC, NH, NJ, NM, NY, OH, OR, PA, SD, TN, TX, WI, WV Foreign: None VA/DOD: None
  • 제품 설명
    EliA Sample Diluent, Article number, 83-1023-01
  • Manufacturer

Manufacturer

  • 제조사 주소
    Phadia US Inc, 4169 Commercial Ave, Portage MI 49002-9701
  • 제조사 모회사 (2017)
  • Source
    USFDA