Retiro De Equipo (Recall) de Horse Blood Agar. 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-2014-RN-01014-1
  • Clase de Riesgo del Evento
    Class III
  • Fecha de inicio del evento
    2014-11-12
  • 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
    Biomerieux have identified the product may contain low level contamination in some plates. contaminants were identified as (1) bacillus cereus, (2) hafniaalvei, and (3) staphylococcus epidermidis.
  • Acción
    bioMérieux requested the customers to inspect the above product prior to use and discard any plates found to be contaminated. Complimentary replacement stock has been shipped in the same quantity as originally provided. This action was undertaken prior to approval of the recall strategy by the TGA.

Device

  • Modelo / Serial
    Horse Blood Agar. An in vitro Diagnostic Medical Device (IVD)Product Reference: 04059Batch Number: EHU-302Expiry Date: 2014-10-23ARTG Number: 201986
  • Manufacturer

Manufacturer