Retiro De Equipo (Recall) de Hospira GemStar Infusion pumps

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 Hospira Inc.

¿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
    14343
  • Fecha de inicio del evento
    2013-04-03
  • 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.
    ICU Medical, Inc. acquired from Pfizer in early 2017, Hospira Infusion Systems, the portion of Hospira dedicated to develop infusion pumps.
  • Notas adicionales en la data
    Recalling Organisation: Hospira NZ Ltd, 58 Richard Pearse Drive, Airport Oaks, Mangere, Auckland 2022
  • Causa
    During infusions at flow rates of 1ml/hr or less, the motor assembly may rotate backwards (roll-back), capturing additional medication that will be delivered resulting in over-infusion. additionally, users may receive x09/001 backward motor movement alarms during the device's power on self test (post) or during an infusion. this alarm will invoke visual and audible warnings to the user and the infusion will not begin or stop, resulting in a delay or interruption in therapy.
  • Acción
    Instructions for use to be updated

Device

  • Modelo / Serial
    Model: All models, Affected: All serial numbers
  • Manufacturer

Manufacturer

  • Empresa matriz del fabricante (2017)
  • Source
    NZMMDSA