Events

Retiro De Equipo (Recall) de Shigella dysenteriae Polyvalent (1 – 10) Agglutinating Serum (reagent intended for the identification of Shigella dysenteriae). 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 Oxoid 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-00868-1
  • Clase de Riesgo del Evento
    Class II
  • Fecha de inicio del evento
    2014-08-06
  • País del evento
    Australia
  • Fuente del evento
    DHTGA
  • URL de la fuente del evento
    https://apps.tga.gov.au/Prod/sara/arn-detail.aspx?k=RC-2014-RN-00868-1
  • 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
    An internal technical investigation by the manufacturer has identified that the listed lot numbers of shigella dysenteriae polyvalent (1-10) agglutinating serum may react with negative isolates, resulting in false positive results.
  • Acción
    Oxoid Australia Pty Ltd is recalling the affected batches of product. End users are requested to inspect their stocks and remove from further use all units from the above lot numbers. The requirement for review of patient results should be determined by the laboratory director. This action has been closed-out on 03/06/2016.

Device

Shigella dysenteriae Polyvalent (1 – 10) Agglutinating Serum (reagent intended for the identifica...
  • Modelo / Serial
    Shigella dysenteriae Polyvalent (1 – 10) Agglutinating Serum (reagent intended for the identification of Shigella dysenteriae). An in vitro diagnostic medical device (IVD)Product Code: R30163701Carton Lot Number: 1111470Bottle Lot Number: 1130078Carton Lot Number: 1236726Bottle Lot Number: 1297592
  • Manufacturer
    Oxoid Australia Pty Ltd

Manufacturer

Oxoid Australia Pty Ltd