Retiro De Equipo (Recall) de Cook Lunderquist Wire Guide

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 William Cook Europe ApS.

¿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
    18738
  • Fecha de inicio del evento
    2015-07-07
  • País del evento
  • Fuente del evento
    NZMMDSA
  • 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: Obex Medical Ltd, 303 Manukau Road, Epsom, AUCKLAND
  • Causa
    Cook medical has received 3 reports of products with the product label indicating the wire guide is curved (the letter "c" in the prefix tscmg- stands for curved), however actual product inside package is a straight wire guide., this observation was made prior to use of the product as the physician is able to see the wire is not curved. the instructions for use (ifu) state "upon removal from package, inspect the product to ensure no damage has occurred.".
  • Acción
    Product to be returned to supplier

Device

Manufacturer