Retiro De Equipo (Recall) de Liberty Tourniquet Green

Según New Zealand Medicines and Medical Devices Safety Authority, este evento ( retiro de equipo (recall) ) involucró a un dispositivo médico en New Zealand que fue producido por Shanghai Lord International Trade Co 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
  • Fecha de inicio del evento
  • País del evento
  • Fuente del evento
  • URL de la fuente del evento
  • Notas / Alertas
    Data from New Zealand is current through July 2018. All of the data comes from the New Zealand Medicines and Medical Devices Safety Authority, 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 New Zealand.
  • Notas adicionales en la data
    Recalling Organisation: Paragon Medical Ltd t/a LR Instruments and Scanmedics, c/o MediRay, 53-55 Paul Matthews Road, Albany, Auckland 0632
  • Causa
    The performance of the liberty green touniquet was identified as faulty. upon examination of three returned items the tourniquets were found to twist when it was tightened resulting in making it harder to release the tourniquet., the stock from ebos healtrhcare has been quarantined and will be returned to head office.
  • Acción
    Product to be returned to supplier