Alerta De Seguridad para Commercial Name: CELLPACK D Technical Name: CAPS, DILUENTS AND OTHER SOLUTIONS FOR LABORATORY ANALYSIS ANVISA Registration Number: 80015490090 Hazard Class: I Model Affected: CELLPACK DCL Serial Numbers Affected: P5016 - SOLE LOT WITH THE ABOVE PROBLEM.

Según Agência Nacional de Vigilância Sanitária (ANVISA), este evento ( alerta de seguridad ) involucró a un dispositivo médico en Brazil que fue producido por SYSMEX DO BRASIL INDÚSTRIA E COMÉRCIO LTDA.; SYSMEX DO BRASIL INDÚSTRIA E COMÉRCIO LTDA..

¿Qué es esto?

Las alertas proporcionan información importante y recomendaciones sobre los productos. Aunque se haya emitido una alerta, esto no significa necesariamente que el producto se considera peligroso. Las alertas de seguridad, dirigidas a trabajadores de la salud y a usuarios, pueden incluir retiro de equipos. Pueden ser escritas por los fabricantes, pero también por funcionarios del área de salud.

Más información acerca de la data acá
  • Tipo de evento
    Safety alert
  • ID del evento
    2178
  • Fecha
    2016-10-15
  • País del evento
  • Fuente del evento
    ANVISA
  • URL de la fuente del evento
  • Notas / Alertas
    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.
  • Notas adicionales en la data
    THE CUSTOMERS WHO PURCHASED THIS PRODUCT LOT WERE CONTACTED THROUGH E-MAIL AND POSSIBLE TELEPHONE CONNECTION, EXPLAINING THE INUTILIZATION OF THE LOTS ACQUIRED WITH THE ABOVE SUPRACITED PROBLEM, WHICH CONSISTS OF THE COMPLETE DISCARACTERIZATION OF THE HEALTH PRODUCT; BEYOND REFUND OF PRODUCTS. THE CUSTOMERS WERE INFORMED THAT THE USE OF THE PRODUCT DOES NOT INTERFERE IN THE QUALITY AND QUANTITY OF THE DIAGNOSTIC TESTS, AND THAT SUCH STATUS OF DISPOSAL OF PRODUCTS, APPLIES FOR PRIMAR FOR THE SAFETY AND TRACEABILITY OF THE BATCH IN QUESTION. LETTER OF COMMUNICATION WITH THE RECOMMENDATIONS TO THE CUSTOMER IN ANNEX.
  • Causa
    Sysmex of brazil of brazil taken science of a divergence in the secondary packaging pack of the product cellpack dcl (dcl-300a), diluente para serie xn. . cabin (secondary packaging) indicates the product cellpack (pk-30l), diluent for series x. but, the same label and the oxygen reagent contained in the package correspond to the cellpack dcl (dcl-300a) product. the failure in the secondary packaging does not interfere in the final quality of the product or the diagnostic test.
  • Acción
    Field Action Code RC0109 triggered under the responsibility of the company SYSMEX DO BRASIL INDÚSTRIA E COMÉRCIO LTDA.