Events

Retiro De Equipo (Recall) de Device Recall Stat Profile Prime Abg AnalyzerStat Profile Prime CCS AnalyzerNova Stat Profile Prime CCS Analyzer

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 Nova Biomedical Corporation.

¿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
    77532
  • Clase de Riesgo del Evento
    Class 2
  • Número del evento
    Z-2732-2017
  • Fecha de inicio del evento
    2017-06-19
  • Estado del evento
    Open, Classified
  • País del evento
    United States
  • Fuente del evento
    USFDA
  • URL de la fuente del evento
    https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfres/res.cfm?id=156306
  • 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
    Electrode measurement, blood-gases (pco2, po2) and blood ph - Product Code CHL
  • Causa
    Software- scheduled a-qc analysis could initiate prior to a patient result being released by the operator and result in the pending patient result being overwritten with the a-qc test results.
  • Acción
    Nova Biomedical issued Urgent Field Correction Notice on June 19, 2017, to all affected customers. The letter advises users of the problem and Nova Biomedical or an authorized Nova Biomedical representative will schedule a no charge update of your Stat Profile Prime Analyzer software to version VI1.0.883.0. A representative will contact customers to schedule this update. Questions: contact Nova Biomedical Technical Support at 1-800-545-6682, in Canada contact us at 1-800-263-5999, or outside of N. America contact your authorized Nova Biomedical subsidiary or distributor. For questions regarding this recall call 781-647-3700.

Device

Device Recall Stat Profile Prime Abg AnalyzerStat Profile Prime CCS AnalyzerNova Stat Profile Pr...
  • Modelo / Serial
    All current software versions
  • Clasificación del producto
    Clinical Chemistry and Clinical Toxicology Devices
  • Clase de dispositivo
    2
  • ¿Implante?
    No
  • Distribución
    Worldwide Distribution - US (Nationwide) Foreign: Albania Algeria Argentina Australia Austria Bangladesh Benin Bolivia Brazil Canada Chile China Colombia Costa Rica Czech Republic ECUADOR Egypt El Salvador Finland France Germany Ghana Greece Guatemala Guyana Honduras Hong Kong Hungary ICELAND India Iran Israel Italy Ivory Coast Japan Jordan Kenya Korea Latvia Macedonia Malaysia Mexico Nepal Netherlands Nigeria Pakistan Pakistan Palestine Peru Philippines Poland Puerto Rico Republic of Panama Republica Dominicana Russia Saudi Arabia Slovak Republic Slovenia South Africa Sri Lanka Switzerland Taiwan Thailand The Netherlands Trinidad,W.I. Tunisia Turkey UK Uruguay Vietnam
  • Descripción del producto
    Nova Biomedical Stat Profile Prime Analyzer as follows: || PN 52855 Stat Profile Prime ABG Analyzer || PN 53655 Stat Profile Prime ABG Analyzer with Scanner || PN 52856 Stat Profile Prime CCS Analyzer || PN 53656 Stat Profile Prime CCS Analyzer with Scanner || PN 53657 Stat Profile Prime CCS Comp Analyzer with Scanner || PN 52857 Stat Profile Prime CCS Comp Analyzer || Blood Gas/Electrolyte/Metabolite/CO-Oximetry Analyzer
  • Manufacturer
    Nova Biomedical Corporation

Manufacturer

Nova Biomedical Corporation
  • Dirección del fabricante
    Nova Biomedical Corporation, 200 Prospect St, Waltham MA 02453-3457
  • Empresa matriz del fabricante (2017)
    Nova Biomedical Corporation
  • Source
    USFDA