Events

Alerta De Seguridad para Cobas p 512 Pre-Analytical System, records 10287411043 and 10287410844, hazard class I, various series: 4700920; 4701020; 4701430; 4706631; 4706731; 4706831; 4706931; 4707031; 4707131; 4707231; 4707331; 4707431; 4707631; 4707831; 4708131; 4709431; 4709531; 4709631; 4709731; 4709831; 4709931; 4,710,231; 4,710,331; 4,714,441; 4,717,943; 4,719,644; 4,725,245; 4,725,345; 4,762,545; 4,727,745; 4,728,145; 4,728,245; 4,728,545; 4,730,345; 4,730,645; 4,732,745; 4,733,045; 4733245; 4,733,645; 4,733,745; 4,733,845; 4,734045; 4,735,345.

Según Agência Nacional de Vigilância Sanitária (ANVISA), este evento ( alerta de seguridad ) involucró a un dispositivo médico en Brazil que fue producido por Roche Diagnóstica Brasil Ltda.; Roche Diagnostics GmBH.

¿Qué es esto?

Las alertas proporcionan información importante y recomendaciones sobre los productos. Aunque se haya emitido una alerta, esto no significa necesariamente que el producto se considera peligroso. Las alertas de seguridad, dirigidas a trabajadores de la salud y a usuarios, pueden incluir retiro de equipos. Pueden ser escritas por los fabricantes, pero también por funcionarios del área de salud.

Más información acerca de la data acá
  • Tipo de evento
    Safety alert
  • ID del evento
    1832
  • Fecha
    2016-03-04
  • País del evento
    Brazil
  • Fuente del evento
    ANVISA
  • URL de la fuente del evento
    http://www.anvisa.gov.br/sistec/alerta/consultaralerta.asp
  • Notas / Alertas
    Brazilian data is current through June 2018. All of the data comes from Anvisa, except for the categories Manufacturer Parent Company and Product Classification.
    The Parent Company and the Product Classification were added by ICIJ.
    The parent company information is based on 2017 public records. The device classification information comes from FDA’s Product Classification by Review Panel, based on matches of data from the U.S. and Brazil.
  • Notas adicionales en la data
    Actions to be taken by the client / user: It was recommended to consider that: The implementation of the software correction is mandatory for the affected systems and will be installed by a Roche Diagnostica Brasil Representative. Until the software fix is ​​implemented, it was recommended that the client / operator monitor the system for the missing tube error 140. If the described situation occurs, all components in contact with the spill must undergo an extra cleaning, as described in the operator's manual. #### Update of the field action: UPDATED ON 10/27/2017, the company presented the report of completion of the field action, with sending of necessary evidences and corrective actions.
  • Causa
    Roche diagnostics gmbh, the legal manufacturer of the product involved in this notification, after a complaint reported abroad, identified the need to update and correct the software of the cobas p 512 pre-analytical system. such modification is necessary because of the incorrect insertion of (rtt), generating risk of contamination of the system and other samples, in addition to loss of material for analysis. so far, this problem has occurred in only three systems of about 400 systems installed in the world. in brazil, no similar complaint has been reported so far.
  • Acción
    Action code SBN_CPS_2016_01. Send letter elaborated on 02/26/2016 of communication to affected clients //// Implementation of software correction for the equipment. If you have any questions regarding this action call 0800-7720295

Device

Cobas p 512 Pre-Analytical System, records 10287411043 and 10287410844, hazard class I, various s...

Manufacturer

Roche Diagnóstica Brasil Ltda.; Roche Diagnostics GmBH