Events

Retiro De Equipo (Recall) de Innova 21211Q/31311Q Biplane Cardiovascular Imaging System.

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 GE Medical Systems, LLC.

¿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
    53596
  • Clase de Riesgo del Evento
    Class 2
  • Número del evento
    Z-0540-2010
  • Fecha de inicio del evento
    2009-10-14
  • Fecha de publicación del evento
    2009-12-16
  • Estado del evento
    Terminated
  • País del evento
    United States
  • Fecha de finalización del evento
    2012-02-04
  • Fuente del evento
    USFDA
  • URL de la fuente del evento
    https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfres/res.cfm?id=85953
  • 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
    Solid state x-ray imager (flat panel/digital imager) - Product Code MQB
  • Causa
    Ge healthcare has become aware of a potential limit switch failure with innova 2121iq and 3131iq (biplane) systems that may impact patient safety. a potential limit switch failure could occur due to collision between the lateral plane of innova positioner and other equipment in the room. this collision may break the x-ray and positioning switches, and may not allow exam completion. to date, no in.
  • Acción
    GE Healthcare issued an "Urgent Medical Device Correction" notice dated October 14, 2009. The letter was addressed to Hospital Administrators/Risk mangers, Managers of Radiology/Cardiology, Radiologists/Cardiologists. The letter described the Safety Issue, Affected Product Details, Safety Instructions, Product Correction and Contact Information. For further information, contact GE Healthcare Systems at 1-800-437-1171, option 4 (U.S.) or contact your local GE Healthcare Service Representative.

Device

Innova 21211Q/31311Q Biplane Cardiovascular Imaging System.
  • Modelo / Serial
    Serial Numbers: 567819BU8 553647BU9 572635BU1 554557BU9 577013BU6 553645BU3 554559BU5 554554BU6 570810BU2 575321BU5 561974BU7 561975BU4 552392BU3 576688BU6 0CLINIC-6 566788BU6 568141BU6 576766BU0 549882BU9 561354BU2 559228BU2 569784BU2 559230BU8 559229BU0 559232BU4 558488BU3 560201BU6 553915BU0 567597BU0 570811BU0 555791BU3 555795BU4 558485BU9 561968BU9 561973BU9 549588BU2 554561BU1 558484BU2 574676BU3 560203BU2 555794BU7 556324BU2 558482BU6 565971BU9 560199BU2 560200BU8 554555BU3 575318BU1 576574BU8 00CLINIC3 556326BU7 556328BU3 555793BU9 555792BU1 558483BU4 561971BU3 558481BU8 553916BU8 570809BU4 566407BU3 567820BU6 573589BU9 553216BU3 559231BU6 553917BU6 561970BU5 561969BU7 577012BU8 561753BU5 551152BU2 549881BU1 556327BU5 00CLINIC4 CLINICAL2 554562BU9 558489BU1 553646BU1 550100BU2 573164BU1 574334BU9 554563BU7 556322BU6 561355BU9 561356BU7 569351BU0 578479BU8 554556BU1 560202BU4 554560BU3 570231BU1 551164BU7 558486BU7 556329BU1 556331BU7 558487BU5 568140BU8 566406BU5 578416BU0 558490BU9 554558BU7 556323BU4 561353BU4 576361BU0 561972BU1 552393BU1 566180BU6 561967BU1 569498BU9 556330BU9 CLINICAL 1 570095BU0 561754BU3 553918BU4 and 556325BU9.
  • Clasificación del producto
    Radiology Devices
  • Clase de dispositivo
    2
  • ¿Implante?
    No
  • Distribución
    Worldwide Distribution -- Including the UNITED STATES, YEMEN, UNITED KINGDOM, TAIWAN, SINGAPORE, RUSSIA, ROMANIA, MALAYSIA, LYB IA, JAPAN, ITALY, IRELAND, INDONESIA, INDIA, GERMANY, FRANCE, EGYPT, CHILE , CANADA and BAHRAIN.
  • Descripción del producto
    GE Healthcare, Innova 2121-1Q/3131-1Q Biplane Cardiovascular Imaging Systems. || Indicated for use in generating fluoroscopic images of human anatomy for vascular angiography, diagnostic and interventional procedures, and optionally, rotational angiography procedures. They are also indicated for generating fluoroscopic images of human anatomy for cardiology, diagnostic, and interventional procedures.
  • Manufacturer
    GE Medical Systems, LLC

Manufacturer

GE Medical Systems, LLC
  • Dirección del fabricante
    GE Medical Systems, LLC, 3000 N Grandview Blvd, Waukesha WI 53188-1615
  • Empresa matriz del fabricante (2017)
    General Electric Company
  • Source
    USFDA