D10 Hemoglobin A1c Program Reorder Pack: 400 tests 의 리콜

U.S. Food and Drug Administration에 따르면, 해당 리콜 는 United States 에서 Bio-Rad Laboratories, 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
    59868
  • 사례 위험등급
    Class 3
  • 사례 연번
    Z-0017-2012
  • 사례 시작날짜
    2011-09-12
  • 사례 출판 날짜
    2011-10-07
  • 사례 상황
    Terminated
  • 사례 국가
  • 사례 종료 날짜
    2012-05-11
  • 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
    Assay, glycoslylated hemoglobin - Product Code LCP
  • 원인
    A previous recall related to reports of calibration failure and late retention times using elution buffer led to an examination of other buffers manufactured during the same time period and a decision was made to field correct these products until a definitive root cause and corrective action have been found and implemented.
  • 조치
    Bio-Rad sent an Urgent Medical Device Correction letter on September 12, 2011, to all affected subsidiaries and customers. The letter identified the product, the problem, and the action to be taken by the customer. Customers were instructed to discard all affected product in accordance with all local, state and federal disposal procedures. If customers distributed the product further they should direct their customers to discard all unused product. Customers were asked to please translate (if necessary) the attached "Customer Medical Device Correction Response Form," customers should add their local contact information and distribute to all affected customers in their region by mail or fax. Compile tracking documentation (e.g. Excel spreadsheet) for all customers who received the Medical Device Correction Letter. Complete the "SUBSIDIARY MEDICAL DEVICE CORRECTION RESPONSE FORM" and fax to Bio-Rad Regulatory Affairs at (510) 741-3954, or e-mail PDF to CSD_RA/Hercules/US/BIO-RAD. Customers would be issued credits for the affected products based on their request. For questions call (510) 741-3954.

Device

  • 모델명 / 제조번호(시리얼번호)
    Model number: 220-0101; Lot number/Expiry: 20010946. 11/30/12; 20011075, 11/30/12;  Contain Buffer lot AA10888/AA10889, expiry 3/31/13;  20011077, 11/30/12; 20011079, 11/30/12; 20011081, 11/30/12. Contain Buffer lot AA10440/AA10441, expiry 2/28/13.
  • 의료기기 분류등급
  • 의료기기 등급
    2
  • 이식된 장치?
    No
  • 유통
    Nationwide and to New Zealand, Canada, France, England, China, India, Mexico, Italy, Brazil, Australia, Singapore, Thailand, SriLanka, hong Kong, Sweden, Germany, Peru, Jamaica, Uruguay, Columbia, Argentina, Chile, Paraguay and Korea.
  • 제품 설명
    D-10 Hemoglobin A1c Program Reorder Pack; 400 tests; || For the determination of Hemoglobin A1c in human whole blood. IVD || Contents: || 1. Elution Buffer 1 2 x 2000 ml Bio-Tris Phosphate Buffer || 2. Elution Buffer 2 1 x 1000 ml Bio-Tris Phosphate Buffer || 3. Wash/Diluent 1 x 1600 mL Deionized water || 4. Analytical cartridge - 1 cation exchange cartridge || 5. Floppy Diskette 1-program parameters || 6. Calibrator/Diluent set. 2 levels of calibrator, 3 vial each: lyophylized human blood cell hemolysate with preservative; 1 bottle 100 mL or diluent deionized water. || 7. Whole Blood Primer: 4 vials Lyophylized human red blood cells hemolysate with preservative. || 8. Sample vials, 100 x 1.5 mL Polypropylene with pierceable lid || 9 Thermal paper - 1 roll || 10. Instruction manual || Made in United States || Bio-Rad Laboratories, Hercules, CA 94547. || Percentage determination of hemoglobin A1c in human whole blood using ion-exchange high=performance liquid chromatography (HPLC)
  • Manufacturer

Manufacturer

  • 제조사 주소
    Bio-Rad Laboratories, Inc., 4000 Alfred Nobel Drive, Hercules CA 94547-1803
  • 제조사 모회사 (2017)
  • Source
    USFDA