Alerte De Sécurité sur Magnetic Resonance Imaging System, Model: DISCOVERY MR450 - Registration 80071260116 - Serial Numbers: This correction applies to all GE Healthcare magnetic resonance imaging (MRI) systems with superconducting magnets.

Selon Agência Nacional de Vigilância Sanitária (ANVISA), ce/cet/cette alerte de sécurité concerne un dispositif en/au/aux/à Brazil qui a été fabriqué par GE Healthcare do Brasil, Com. e Serv. para Equipamentos Médicos-Hospitalares Ltda.; GE MEDICAL SYSTEMS, LLC.

Qu'est-ce que c'est?

Les alertes fournissent des informations importantes et des recommandations concernant les dispositifs médicaux. Le fait qu'une alerte soit émise ne signifie pas nécessairement qu'un dispositif soit dangereux. Les alertes de sécurité, qui sont envoyées tant aux travailleurs du secteur médical qu'aux utilisateurs de ces dispositifs, peuvent inclure des rappels. Elles peuvent être rédigées par des fabricants mais aussi par des autorités en charge de la santé.

En savoir plus sur les données ici
  • Type d'événement
    Safety alert
  • ID de l'événement
    1501
  • Date
    2015-01-26
  • Pays de l'événement
  • Source de l'événement
    ANVISA
  • URL de la source de l'événement
  • Notes / Alertes
    Brazilian data is current through June 2018. All of the data comes from Anvisa, 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 Brazil.
  • Notes supplémentaires dans les données
    The company informs that the Magnetic Field Deactivation Module (MRU) is a fundamental safety component of the magnetic resonance (MR) system that generates the magneto quench (ie, causes it to become non- magnetic) in emergency situations, such as may occur when a ferromagnetic object is brought into the magnetic field.
  • Cause
    The company informs that there is a possibility that the mru is not connected to the magnet. if the mru is turned off, it will not work as expected and will not generate the quench on the magnet when the button is pressed. in emergencies, the disconnected mru could delay the removal of a ferromagnetic object from the magnet, potentially resulting in serious injuries.
  • Action
    As a precautionary measure, users should confirm that the MRU is connected to the magnet by performing the following four-step test in the MRU: 1. Verify that the green Charger Power LED is lit. 2. Press and hold the BATTERY TEST button (Test Battery) for 15 seconds. The green BATTERY TEST LED should light up and remain lit while the BATTERY TEST button is pressed. 3. Set the HEATER TEST switch (Test Heater) to position A. The green HEATER TEST LED should light up. If it does not light up, press the HEAT TEST LED (Test Heater LED) button to verify that the LED is working. 4. Set the HEATER TEST switch to position B. The green HEATER TEST LED should light up. If it does not light up, press the HEATING LED TEST button to verify that the LED is working. If the MRU test does not work as described in each of the 4 steps above, users should stop using the system and call the GE Healthcare representative immediately for correction. Users should also refer to the Safety Manual for precautions regarding the handling of ferromagnetic material around high magnetic fields. Users should be familiar with routine inspections and maintenance of the safety features of the system and the various methods that can be used if magnetic field quench is required. All of this information is documented in the Safety Manual provided with the MRI (Magnetic Resonance Imaging) system.