Retiro De Equipo (Recall) de NucliSENS easyMAG Magnetic Silica MagSIL (used with the NucliSENS easyMag nucleic acid extraction system for the automated extraction of total nucleic acids (RNA/DNA) from biological samples). An in vitro diagnostic medical device (IVD)

Según Department of Health, Therapeutic Goods Administration, este evento ( retiro de equipo (recall) ) involucró a un dispositivo médico en Australia que fue producido por Biomerieux Australia Pty Ltd.

¿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
    RC-2016-RN-00949-1
  • Clase de Riesgo del Evento
    Class I
  • Fecha de inicio del evento
    2016-07-20
  • País del evento
  • Fuente del evento
    DHTGA
  • URL de la fuente del evento
  • Notas / Alertas
    Australian data is current through July 2018. All of the data comes from the Australian Therapeutic Goods Administration, 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 recall data from the U.S. and Australia.
  • Notas adicionales en la data
  • Causa
    Following customer complaints about amplification performance issues with home brew pcr and rt- pcr assays, biomérieux investigation has confirmed an issue with specific batches of magnetic silica (ref: 280133). the investigation concluded that downstream applications were impacted when the extraction volume was higher than 400µl and for double stranded nucleic acids target. double stranded nucleic acid applications with small (< 40kbp) and medium genome sizes (< to 1200 kbp) i.E., dna viruses are more impacted than higher human genomic dna and bacterial applications (> to 1200kbp).This may result in false negative, invalid or under-quantification of results. if invalid results are obtained, it could lead to a delayed result until a new run or a new extraction is performed.
  • Acción
    bioMérieux is advising users to ensure controls with the same nature/structure as the target and/or external controls are used to detect the issue. Users are advised to reduce the sample input volume to 200µL, until the silica problems is resolved. Downstream ARGENE and NucliSENS easyQ HIV 1 V2.0 applications performed according to the IFU are not affected. It is recommended that the continued use with blood transfusion testing with confirmed by the Laboratory Director, and to discuss any concerns regarding previously reported results with the Laboratory Director.

Device

  • Modelo / Serial
    NucliSENS easyMAG Magnetic Silica MagSIL (used with the NucliSENS easyMag nucleic acid extraction system for the automated extraction of total nucleic acids (RNA/DNA) from biological samples). An in vitro diagnostic medical device (IVD)Catalogue Number: 280133Lot Numbers:Z017BB1MS, Z017BF1MS, Z017BA1MS Expiry Date: 28/02/2017Z017CC1MS, Z017CG1MS Expiry Date: 28/03/2017Z017DC1MS, Z017DD1MSExpiry Date: 28/04/2017ARTG Number: 240760
  • Manufacturer

Manufacturer