Events

Retiro De Equipo (Recall) de Device Recall AVOXimeter 1000, AVOXimeter 4000

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 International Technidyne Corp..

¿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
    58549
  • Clase de Riesgo del Evento
    Class 2
  • Número del evento
    Z-2218-2011
  • Fecha de inicio del evento
    2011-03-23
  • Fecha de publicación del evento
    2011-05-19
  • Estado del evento
    Terminated
  • País del evento
    United States
  • Fecha de finalización del evento
    2012-10-25
  • Fuente del evento
    USFDA
  • URL de la fuente del evento
    https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfres/res.cfm?id=99574
  • 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
    Spectral, absorb, curve, oryhemoglobin, carboxyhemoglobin, carbon monoxide - Product Code DQA
  • Causa
    An incorrect calibration code that affects the total hemoglobin measurement was applied to affected avoximeter instruments.
  • Acción
    International Technidyne Corp. sent a letter dated March 23, 2011, to all affected customers. The letter identified the product, the problem, and the action to be taken by the customer. Customers were instructed to check their inventory to determine if they have any of the affected product. If they have any of the affected product, customers were instructed to stop using it and remove it from their inventory. Customers were also instructed to complete the attached Customer Account Tracking Form and return it by fax to (732-635-0144) or e-mail (techsupport@itcmed.com) or mail to: ITC Technical Support 20 Corporate Place South Piscataway, New Jersey 08854 For any questions call the Distributor or ITC Nexus Dx Technical Support at 800-631-5945 (US) or 732-548-5700 (International), ext 4707.

Device

Device Recall AVOXimeter 1000, AVOXimeter 4000
  • Modelo / Serial
    AVOXimeter 1000: K922075 AVOX1000, AVOX1000E-110, AVOX1000INT  AVOXimeter 4000: K951485 AVOX4000, AVOX4000D
  • Clasificación del producto
    Anesthesiology Devices
  • Clase de dispositivo
    2
  • ¿Implante?
    No
  • Distribución
    Worldwide Distribution - USA including TX, KS, OH, OR, FL, GA, NY, MA, and DC and the countries of Taiwan and Thailand
  • Descripción del producto
    AVOXimeter 1000, AVOXimeter 4000 || 1000- portable bedside whole blood oximeter that directly measures oxyhemoglobin fraction, the total hemoglobin concentration, and oxygen content. It has enhanced software that optimizes its use int he cardiac catheterization laboratory through calculations of physiologic equations. 4000-a portable bedside whole blood CO-oximeter that directly measures total hemoglobin concentration and the relative concentrations of oxyhemoglobin carboxyhemoglobin concentration methemoglobin. In addition, oxygen content oxygen capacity and oxygen saturation indices are calculated.
  • Manufacturer
    International Technidyne Corp.

Manufacturer

International Technidyne Corp.
  • Dirección del fabricante
    International Technidyne Corp., 68 Olsen Ave, Edison NJ 08820-2419
  • Empresa matriz del fabricante (2017)
    Werfenlife Sa.
  • Source
    USFDA