Retiro De Equipo (Recall) de Device Recall BD Vacutainer Blood Collection

Según U.S. Food and Drug Administration, este evento ( retiro de equipo (recall) ) involucró a un dispositivo médico en United States que fue producido por Becton Dickinson & Company.

¿Qué es esto?

Una corrección al equipo o acción de retiro tomada por el fabricante para abordar un problema con un dispositivo médico. Los retiros (recalls) ocurren cuando un dispositivo médico está defectuoso, cuando puede poner en riesgo la salud, o cuando simultáneamente está defectuoso y puede poner en riesgo la salud.

Más información acerca de la data acá
  • Tipo de evento
    Recall
  • ID del evento
    35831
  • Clase de Riesgo del Evento
    Class 2
  • Número del evento
    Z-1461-06
  • Fecha de inicio del evento
    2006-06-21
  • Fecha de publicación del evento
    2006-09-09
  • Estado del evento
    Terminated
  • País del evento
  • Fecha de finalización del evento
    2007-06-07
  • Fuente del evento
    USFDA
  • URL de la fuente del evento
  • Notas / Alertas
    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.
  • Notas adicionales en la data
    Vacutainer Blood CollectionBlood Collection - Product Code FMI
  • Causa
    Firm received complaints indicating failure of the non-patient (np) sleeve to function properly. this sleeve covers the cannula and prevents leakage during blood collection.
  • Acción
    BD sent out recall notifications on 6/21/2006 to distributors and their direct account customers.

Device

  • Modelo / Serial
    Lot numbers: 5326641; 5336280; 5340618; 5341943; 5342548; 5342549; 5348212; 5348215; 5355629; 5357860; 5357891; 6009122; 6020878; 6024334; 6031704; 6040224. For European distribution, the products are shipped to Temse located in Belgium who handles the recall. Temse has been identified as recalling only the following products and lots: Catalog Number 364896 (Direct Draw Adapter), lots 5311376, 5312193, 5312201. Catalog Number 367300 (Luer Adapter), lots 5307894, 5307896, 5307900.
  • Clasificación del producto
  • Clase de dispositivo
    2
  • ¿Implante?
    No
  • Distribución
    World wide-Products are distributed nationwide to distributors and direct accounts. The products are also distributed internationally to the following locations: Japan, Australia, Canada, Hong Kong, New Zealand. For European distribution, the products are shipped to Temse located in Belgium who handles the recall. Temse has been identified as recalling only the following products and lots: Catalog Number 364896 (Direct Draw Adapter), lots 5311376, 5312193, 5312201. Catalog Number 367300 (Luer Adapter), lots 5307894, 5307896, 5307900. Government accounts include the VAMC in Erie, PA;
  • Descripción del producto
    BD Vacutainer Blood Collection Assembly with BD Blunt Plastic Cannula; Catalog #303380.
  • Manufacturer

Manufacturer

  • Dirección del fabricante
    Becton Dickinson & Company, 1 Becton Dr, Franklin Lakes NJ 07417-1815
  • Empresa matriz del fabricante (2017)
  • Source
    USFDA