Events

Retiro De Equipo (Recall) de Philips MobileDiagnost wDR1 and 2, resistive arrestor strap

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 Philips Medical Systems DMC GmbH.

¿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
    18689
  • Fecha de inicio del evento
    2015-06-17
  • País del evento
    New Zealand
  • Fuente del evento
    NZMMDSA
  • URL de la fuente del evento
    https://medsafe.govt.nz/hot/Recalls/RecallSearch.asp
  • 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: Philips New Zealand Commercial Limited, Level 3, 123 Carlton Gore Road, Newmarket, AUCKLAND 1023
  • Causa
    When the system is driven over a non-conductive floor and then over a conductive, grounded part, proper control of the drive behavior may not be possible. the system can be stopped by releasing the drive handle. proper behavior is re-enabled when the system is rebooted.
  • Acción
    Product to be modified

Device

Philips MobileDiagnost wDR1 and 2, resistive arrestor strap
  • Modelo / Serial
    Model: Models: wDR1 and wDR2, Affected: All MobileDiagnost wDR 1 with serial number lower than 15000005 and all MobileDiagnost wDR 2 with serial number lower than 15100050
  • Manufacturer
    Philips Medical Systems DMC GmbH

Manufacturer

Philips Medical Systems DMC GmbH
  • Empresa matriz del fabricante (2017)
    Philips
  • Source
    NZMMDSA