Trade name: iChem VELOCITY Technical name: Urine Analyzer Instrument ANVISA Registration Number: 10033129046 Hazard Class: I Affected Model: Serial Numbers Affected: All instrument serial numbers in Brazil are affected by this notification. 의 안전성 경고

Agência Nacional de Vigilância Sanitária (ANVISA)에 따르면, 해당 안전성 경고 는 Brazil 에서 Beckman Coulter do Brasil Comércio e Importação de Produtos para Laboratório Ltda; IRIS Diagnostics a Division of Iris Internacional 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
    2218
  • 날짜
    2017-02-24
  • 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
    • Avoid hitting the probe during maintenance or troubleshooting. • Carefully follow the instructions in the Operator's Manual, PN 301-7146 or 300-4449, to: - Use the Probe Safety Latch. - Use approved pipe types. - Remove tube caps prior to sample analysis to avoid probe-tube collisions. • As a temporary measure, perform a patient cross-check or perform QA after performing maintenance or troubleshooting in the sample probe area. If you have any questions about the results, please contact our Customer Service Center. • Consult the Laboratory Director to determine if a retrospective review of the results is medically justified.
  • 원인
    On 31.01.2017, beckman coulter of brazil received beckman coulter inc. from its parent company, an email with an urgent medical device recall notification, stating that iris international has determined that misalignment of the sample probe or probe damaged in ichemvelocity can lead to a remote possibility of falsely negative results due to improper dosing of the strip. the investigation was initiated on the basis of customer complaints for control failures.
  • 조치
    Field Action Code FA-17006 triggered under the responsibility of Beckman Coulter of Brazil Trade and Import of Products for Laboratório Ltda. Company will make correction in the field.