VITROS * FOR PHENITOIN PHYT Technical Name: PHENYTOIN ANVISA Registration Number: 10132590219 Hazard Class: II Affected Model: VITROS * DRY REACTIVE FOR PHYTENIN PHENITOIN 5 cartridges with 18 slides VITROS Chemistry Products PHYT Slides , product code 8298671, lots: 1401566241, 1401566904, 1401577639, 1401578552, 1401578552, 1401580410, 1401589627, 1401591230, 1401592935, 1401604105 and 1401614738. The Assay Data Diskette (ADD) and Calibration 16607 products are not applicable. 의 안전성 경고

Agência Nacional de Vigilância Sanitária (ANVISA)에 따르면, 해당 안전성 경고 는 Brazil 에서 Johnson & Johnson do Brasil Ind. e Com. de Prod. para Saúde Ltda; Ortho-Clinical Diagnostics, Inc. 에 의해 제조된 제품과 관련되어 있습니다.

이것은 무엇인가요?

안전성 경고는 의료기기 제품과 관련된 중요한 정보와 권고사항을 담고 있습니다. 물론 안전성 경고가 배포되었다고 해서 해당 제품이 무조건 안전하지 않은 제품이라는 것은 아닙니다. 보건의료업계 종사자와 의료기기 사용자들에게 배포되는 안전성 경고에는 회수(recall)도 포함될 수 있습니다. 제조사가 안전성 경고를 작성하기도 하지만, 보건당국에서 작성하는 경우도 있습니다.

데이터에 대해 더 자세히 알아보기 여기
  • 사례 유형
    Safety alert
  • 사례 ID
    2107
  • 날짜
    2016-12-18
  • 사례 국가
  • 사례 출처
    ANVISA
  • 사례 출처 URL
  • 비고 / 경고
    Brazilian data is current through June 2018. All of the data comes from Anvisa, except for the categories Manufacturer Parent Company and Product Classification.
    The Parent Company and the Product Classification were added by ICIJ.
    The parent company information is based on 2017 public records. The device classification information comes from FDA’s Product Classification by Review Panel, based on matches of data from the U.S. and Brazil.
  • 데이터 추가 비고
    Some instructions are recommended: 1) Install the Calibration Diskette / ADD DRV 5910 or later diskette in the system: The automatic download will be available for the e-Connected systems as of December 2, 2016; The Calibration Diskette and / or ADD diskette will also be sent to your installation upon availability. IMPORTANT NOTE: After charging the DRV 5910 (or later) for the first time, VITROS PHYT Slides will lose calibration and recalibrate. In the meantime, it is acceptable to continue using the product. 2) After successful calibration and quality control evaluation, it is acceptable to use existing inventory of VITROS PHYT Slides. 3) Place this notification on the VITROS System or along with the user documentation. 4) Fill out and return the Receipt Confirmation Form.
  • 원인
    This notice provides additional information from a product correction notification that ortho clinical diagnostics (ortho) issued in december 2015 regarding clarification of the operator's actions for laundering errors. since then, the occurrence of u90-382 or 6lu condition codes associated with wash errors has been monitored and an increase in wash errors has been observed for vitros chemistry products phyt slides.
  • 조치
    Field Action Code 16000169 triggered under the responsibility of Johnson & Johnson do Brasil Ind. And Com. De Prod. for Health Ltda. Company will make correction in the field.