Events

Retiro De Equipo (Recall) de VITROS 5600

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 Ortho-Clinical Diagnostics.

¿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
    60881
  • Clase de Riesgo del Evento
    Class 3
  • Número del evento
    Z-1073-2012
  • Fecha de inicio del evento
    2011-04-13
  • Fecha de publicación del evento
    2012-02-21
  • Estado del evento
    Terminated
  • País del evento
    United States
  • Fecha de finalización del evento
    2016-05-09
  • Fuente del evento
    USFDA
  • URL de la fuente del evento
    https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfres/res.cfm?id=106705
  • 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
    Ortho clinical diagnostics (ocd) received customer complaints regarding the loss of calibration data following the installation of a development assay data disk (add) that was available in the on-screen mailbox on the main menu system status screen of their vitros¿ 5600 integrated system. ocd's investigation determined that add, data release version (drv) 9241 or 9251 was electronically transferr.
  • Acción
    Ortho-Clinical Diagnostics (OCD) sent an Important Product Correction Notification letters dated April 13, 2011 via FedEx overnight to customers with an affected VITROS¿ 3600 or 5600 System (those not e-Connected). Foreign affiliate consignees were informed of this action via e-mail on April 13, 2011. The letters described the affected products, problem and actions to be followed. The letters states that an OCD Field Engineer will contact customers who has the affected products and perform a Modification (MOD) procedure that will remove ADD DRV 9241 or 9251 from the on-screen mailbox of their system(s). Customers were instructed to complete and return the accompanying Confirmation of Receipt Form and fax to1-888-557-3759 or 1-585-453-4110. The letter asks that distributors forward a copy of the enclosed customer communication to all customers who were shipped an affected VITROS¿ 3600 or 5600 System. For questions, please contact OCD's Customer Technical Services at 1-800-421-3311.

Device

VITROS 5600
  • Modelo / Serial
    All VITROS¿ 5600 Systems Catalog # 6802413 that have not been eConnected which may have Assay Data Disk (ADD) Data Release Version (DRV) 9241 or 9251. J/Serial Numbers: 56000395, 56000482, 56000497,  56000511, 56000514, 56000524, 56000553, 56000607, 56000608, 56000770, 56000776, 56000777, 56000778, 56000824, 56000825, 56000826, 56000827, 56000835, 56000840, 56000841, 56000843, 56000888, 56000892, 56000902, 56000905, 56000927, 56000954, 56000955,  56000974, 56000976, 56000987, 56000990, 56000994, 56000122,  56000124, 56000133, 56000138, 56000187, 56000220, 56000223, 56000286, 56000288, 56000329, 56000353, 56000358, 56000429, 56000431, 56000455, 56000465, 56000487, 56000526, 56000627, 56000664, 56000672, 56000673, 56000674, 56000677, 56000683, 56000685, 56000715, 56000716, 56000723, 56000725, 56000726, 56000730, 56000732, 56000733, 56000734, 56000735, 56000739, 56000754, 56000760, 56000761, 56000762, 56000763, 56000765, 56000766, 56000767, 56000784, 56000789, 56000791, 56000799, 56000804, 56000805, 56000806, 56000807, 56000808, 56000809, 56000828, 56000829, 56000834, 56000862, 56000868, 56000869, 56000870, 56000897, 56000899, 56000916, 56000917, 56000922, 56000931, 56000940, 56000944, 56000946, 56000947, 56000949, 56000956, 56000960, 56000969, 56000986, 56000988, 56000989, 56000998, 56001003, 56001005, 56001006, 56001009, 56001014, 56001017, 56001018, 56001020, 56001030, 56001034, 56001035, 56001036, 56001037, 56001038, 56001039, 56001040, 56001044, 56001045, 56001050. --- NOTE: VITROS¿ 5600 that are e-Connected are not affected by this issue.
  • Clasificación del producto
    Clinical Chemistry and Clinical Toxicology Devices
  • Clase de dispositivo
    1
  • ¿Implante?
    No
  • Distribución
    Worldwide Distribution - USA (nationwide) including the countries of: Brazil, Canada, Chile, China, England, France, Germany, India, Italy, Japan, Mexico, Singapore, Spain and Venezuela.
  • Descripción del producto
    VITROS¿ 5600 Integrated Systems, Catalog # 6802413; COMMON/USUAL NAME: VITROS¿ 5600 --- NOTE: VITROS¿ 5600 that are e-Connected are not affected by this issue. || Product Usage: || For use in the in vitro quantitative, semi-quantitative, and qualitative measurement of a variety of analytes of clinical interest, using VITROS¿ Immunodiagnostic Products Reagents.
  • Manufacturer
    Ortho-Clinical Diagnostics

Manufacturer

Ortho-Clinical Diagnostics
  • Dirección del fabricante
    Ortho-Clinical Diagnostics, 100 Indigo Creek Drive, Rochester NY 14626
  • Source
    USFDA