Retiro De Equipo (Recall) de First Response Digital Pregnancy Test and First Response Test & Reassure. 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 Church and Dwight 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
  • ID del evento
  • Clase de Riesgo del Evento
    Class III
  • Fecha de inicio del evento
  • País del evento
  • Fuente del evento
  • 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
    It has been determined that during consumer use, the internal mechanism of the affected devices is giving an error reading which is shown as "?" on the display. there are no health risks associated with this issue; the device will not give a false positive or false negative result reading.
  • Acción
    Church & Dwight is advising wholesalers to inspect their stock and quarantine affected stock to prevent further sale. Affected stock is to be returned to Cargo Line International. Wholesalers are requested to provide a copy of the recall letter to other warehouses, retail facilities or other organisations to which they have transferred or supplied affected product. Consumers will be provided a full refund, from where they purchased the product or by contacting Church & Dwight Customer Service, for devices from the affected batches that have resulted in an invalid (“?”) reading. This action has been closed-out on 23/06/2017.


  • Modelo / Serial
    First Response Digital Pregnancy Test and First Response Test & Reassure. An in vitro diagnostic medical device (IVD).First Response Digital Pregnancy Test Product Code: 0734Lot Numbers: SU5341 (exp 07/2017), SU6207, SU6237, SU6305A (exp 07/2017), SU6308 (exp 10/2017), SU6335 (exp 10/2017)First Response Test & ReassureProduct Code: 0737Lot Numbers: SU6196 (exp 07/2017), SU6315A (exp 10/2017)ARTG Number: 231933
  • Manufacturer