Events

Retiro De Equipo (Recall) de Device Recall cobas 6000 Series System, cobas 8000 Modular Analyzer Series, cobas c 311 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 Roche Diagnostics 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
    76854
  • Clase de Riesgo del Evento
    Class 2
  • Número del evento
    Z-2049-2017
  • Fecha de inicio del evento
    2017-03-21
  • Estado del evento
    Terminated
  • País del evento
    United States
  • Fecha de finalización del evento
    2017-10-02
  • Fuente del evento
    USFDA
  • URL de la fuente del evento
    https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfres/res.cfm?id=154407
  • 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
    Analyzer, chemistry (photometric, discrete), for clinical use - Product Code JJE
  • Causa
    Due to a design change in 2015, corrosion on the sample probe electrical contacts can occur and lead to a disturbance of the sample liquid level detection (lld). when disturbance of the sample liquid level detection (lld) occurs, the affected sample probe may dip into the sample material deeper than intended. this may lead to carryover and medical risk cannot be excluded.
  • Acción
    On March 21, 2017, URGENT MEDICAL DEVICE RECALL notifications were sent to the affected consignees via courier. The recall notification included a description of the reason for the recall, affected product, consignee responsibilities, and instructions for responding to the formal recall notification.

Device

Device Recall cobas 6000 Series System, cobas 8000 Modular Analyzer Series, cobas c 311 analyzer
  • Modelo / Serial
    sample probe catalog numbers: 04547241001 - cobas c 501/502 05899427001 - cobas c 311 04945794001 - cobas c 701/702 and cobas 8000 ISE  Lot numbers: cobas c 311 0490232027, 0490233855, 0490236427, 0490238543, 0490241937, 0490248322, 0490250880, 0490235713, 0490252029, 0490256963  cobas c 501, c 502 0490233762, 0490233764, 0490233766, 0490233767, 0490233777, 0490235904, 0490235905, 0490235906, 0490235907, 0490235949, 0490235950, 0490237594, 0490237595, 0490237353, 0490237354, 0490237597, 0490237598, 0490237600, 0490237602, 0490237604, 0490237606, 0490238955, 0490238957, 0490238893, 0490238895, 0490238896, 0490238898, 0490238899, 0490242149, 0490242151, 0490242153, 0490242155, 0490242327, 0490242328, 0490242329, 0490242330, 0490242331, 0490250491, 0490250492, 0490250493, 0490250494, 0490250495, 0490250496, 0490251032, 0490251033, 0490251034, 0490251036, 0490252524, 0490252527, 0490252529, 0490252532, 0490252247, 0490252249, 0490252251, 0490252252, 0490252272, 0490252398, 0490254550, 0490254551, 0490254552, 0490254553, 0490254554, 0490254555, 0490254804, 0490254805, 0490254806, 0490254807, 0490256999, 0490257000, 0490256993, 0490256994, 0490256995, 0490256996, 0490256997, 0490256998, 0490254808, 0490257001, 0490257847, 0490257848, 0490257849, 0490257850, 0490257851, 0490258652  cobas c 701, c 702 0490238960, 0490238961, 0490238963, 0490242332, 0490251040, 0490251041, 0490252546, 0490252547, 0490254810, 0490254811, 0490221658, 0490223228, 0490223229, 0490225255, 0490226172, 0490226173, 0490226174, 0490227626, 0490227627, 0490227628, 0490230276, 0490230277, 0490230279, 0490232203, 0490232204, 0490232205, 0490232206, 0490233778, 0490233779, 0490233780, 0490233781, 0490233783, 0490235909, 0490235910, 0490235911, 0490235912, 0490235913, 0490237365, 0490237366, 0490237367, 0490237368, 0490237369, 0490237370, 0490238901, 0490238902, 0490238903, 0490238904, 0490242160, 0490242161, 0490242163, 0490242165, 0490242166, 0490250498, 0490250499, 0490250500, 0490250501, 0490250502, 0490252308, 0490252312, 0490252318, 0490252320, 0490252322, 0490254558, 0490254559, 0490254560, 0490254561, 0490254562, 0490257035, 0490257036, 0490257037, 0490257038, 0490257039, 0490257854, 0490257855, 0490257856, 0490257857, 0490257858
  • Clasificación del producto
    Clinical Chemistry and Clinical Toxicology Devices
  • Clase de dispositivo
    1
  • ¿Implante?
    No
  • Distribución
    US Nationwide.Distribution
  • Descripción del producto
    Sample probes associated with: || cobas 6000 Series System, cobas 8000 Modular Analyzer Series, cobas c 311 analyzer || cobas c 501/502 || cobas c 701/702 || cobas 8000 ISE || Product Usage: || The cobas 6000 series is a fully automated, random-access, software-controlled system for immunoassay and photometric analysis intended for qualitative and quantitative in vitro determinations using a wide variety of tests. It is optimized for high throughput workloads in the professional environment using a combination of Ion selective electrodes (ISE), a photometric analysis unit an immunoassay analysis module. The cobas 8000 Modular Analyzer Series is a fully automated system for Clinical chemistry analysis, intended for the in vitro qualitative and quantitative determination of analytes in body fluids. It is optimized for high throughput workloads in the professional environment using a combination of ion selective electrodes (ISE) and a photometric analysis unit. The cobas c 311 analyzer is an in-vitro diagnostic analyzer capable of performing clinical chemistry, specific protein and electrolyte tests. Analytes are measured photometrically or turbidimetrically; the analyzer also has an optional ISE module for measuring sodium, potassium and chloride.
  • Manufacturer
    Roche Diagnostics Corporation

Manufacturer

Roche Diagnostics Corporation
  • Dirección del fabricante
    Roche Diagnostics Corporation, 9115 Hague Rd, Indianapolis IN 46256-1025
  • Empresa matriz del fabricante (2017)
    Roche Holding AG
  • Source
    USFDA