Events

Retiro De Equipo (Recall) de Device Recall CryoValve

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 Cryolife Inc.

¿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
    27949
  • Clase de Riesgo del Evento
    Class 2
  • Número del evento
    Z-0516-04
  • Fecha de inicio del evento
    2003-11-10
  • Fecha de publicación del evento
    2004-02-10
  • Estado del evento
    Terminated
  • País del evento
    United States
  • Fecha de finalización del evento
    2004-05-06
  • Fuente del evento
    USFDA
  • URL de la fuente del evento
    https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfres/res.cfm?id=30787
  • 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
    Heart-Valve, Allograft - Product Code MIE
  • Causa
    The firm received additional information from the procurement agency indicating that yeast was detected in the musculoskeletal procurement cultures for the hemi pelvis.
  • Acción
    Consignee was first notified by telephone on 11/10/2003, with a follow up letter sent 12/10/2003. If the tissue had been implanted the consignee was advised to forward that information to CryoLife''s Regulatory Department-Field Assurance. If the tissue had not been implanted the consignee was advised not to implant or further distribute the tissue. They were instructed to remove the tissue from the implantable inventory and to place it into quarantine pending return to CryoLife. A self addressed, stamped postcard was included to affirm receipt of notification and to acknowledge that the tissue had been placed into quarantine.

Device

Device Recall CryoValve
  • Modelo / Serial
    Donor number: 71237, Serial number: 8214013, Model number: PV00
  • Clasificación del producto
    Cardiovascular Devices
  • Clase de dispositivo
    3
  • ¿Implante?
    Yes
  • Distribución
    The tissue was issued to one hospital in CA.
  • Descripción del producto
    CryoValve, Pulmonary Valve & Conduit
  • Manufacturer
    Cryolife Inc

Manufacturer

Cryolife Inc
  • Dirección del fabricante
    Cryolife Inc, 1655 Roberts Blvd Nw, Kennesaw GA 30144-3632
  • Source
    USFDA