Notificaciones De Seguridad De Campo acerca de Clinitest® hCG Cassette Pregnancy Test Kit

Según Health Products Regulatory Authority, este evento ( notificaciones de seguridad de campo ) involucró a un dispositivo médico en Ireland que fue producido por Siemens Healthcare Diagnostics.

¿Qué es esto?

Las notificaciones de seguridad de campo son comunicaciones sobre acciones que se pueden estar tomando en relación con un producto que se encuentra en el mercado, enviadas por los fabricantes de dispositivos médicos o sus representantes. Estas notificaciones son principalmente para trabajadores de la salud, pero también para usuarios. Pueden incluir alertas y retiro de equipos.

Más información acerca de la data acá
  • Tipo de evento
    Field Safety Notice
  • Número del evento
    SN2008(05)
  • Fecha
    2008-04-15
  • País del evento
  • Fuente del evento
    HPRA
  • URL de la fuente del evento
  • Notas / Alertas
    "Irish data is current through April 2019. All of the data comes from the Health Products Regulatory Authority (Ireland), 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 Ireland."
  • Notas adicionales en la data
  • Causa
    Lot 97552 and lot 97574 of the clinitest hcg pregnancy test kits has been recalled by the manufacturer due to the potential for false negative results i.E. a negative result obtained in pregnancy.
  • Acción
    Action or Recommendations For Healthcare Professionals    Ensure that all relevant staff in your institution are informed of this recall  Determine if you have lot 97552 and lot 97574 of the above product Locate and cease using product from lot 97552 and lot 97574 Determine how much of this product has been used Follow the distributor / manufacturers recommendations for quarantine and disposal of product Follow up patients as required   Action or Recommendations For Patients Patients who have had a recent pregnancy test in hospital but are concerned that the negative result received may be incorrect should contact or seek a retest from their GP, family planning clinic or pharmacist

Device

Manufacturer

  • Empresa matriz del fabricante (2017)
  • Source
    HPRA