Alerta De Seguridad para ABS2000 COMPUTERIZED BLOOD BANK INSTRUMENTS

Según Agência Nacional de Vigilância Sanitária (ANVISA), este evento ( alerta de seguridad ) involucró a un dispositivo médico en Brazil que fue producido por IMMUCOR INC.

¿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
    61
  • Fecha
    2000-12-13
  • 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
    UNTIL THIS DATE DOES NOT CONSERT PRODUCT REGISTRATION IN BRAZIL
  • Causa
    The safety alarm for the instruments mentioned was removed from the screen and crossmatch analysis; alarm still applies to group analysis. the manufacturer began a recall through correspondence sent on december 13, 2000.
  • Acción
    MAKE SURE YOU HAVE RECEIVED THE CORRESPONDENCE OF DECEMBER 13, 2000 FROM IMMUCOR. IMMUCOR DECLARES THAT UNLIMITED FIELD CORRECTIONS ARE COMPLETED, CUSTOMERS ARE ADVISED TO CONTINUE VALIDATING GROUP RESULTS (ABO / RH) THROUGH AN ALTERNATIVE METHOD. FOR FURTHER INFORMATION, OR TO SCHEDULE CORRECTION, CONTACT IMMUCOR BY TEL. (800) 829-2553 OR BY TEL. (770) 441-2051

Device

Manufacturer

  • Source
    ANVSANVISA