Events

Alerte De Sécurité sur NIM non-invasive nerve monitoring equipment Medtronic Xomed

Selon National Institute of Drugs and Food Surveillance (INVIMA), ce/cet/cette alerte de sécurité concerne un dispositif en/au/aux/à Colombia qui a été fabriqué par Medtronic Xomed, Inc || Medtronic Xomed Instrumentation S.A.S || Medtronic Xomed Inc. || Fidia Advance Biopolymers S.R.L.

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
    I1606-267
  • Numéro de l'événement
    2009DM-0003762
  • Date
    2016-06-30
  • Pays de l'événement
    Colombia
  • Source de l'événement
    INVIMA
  • URL de la source de l'événement
    https://app.invima.gov.co/alertas/dispositivos-medicos-invima?page=134
  • Notes / Alertes
    Colombian data is current through June 2019. All of the data comes from the National Institute of Drugs and Food Surveillance (INVIMA), 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 Colombia.
  • Notes supplémentaires dans les données
  • Cause
    The manufacturer who has identified a problem with excessive flexing of the tube by the user, especially at a sharp or abrupt angle, can cause the electrode wires to flow into its channel in the silicone wall, leading to potential adverse events occurring in patients.

Device

NIM non-invasive nerve monitoring equipment Medtronic Xomed
  • Modèle / numéro de série
    Endotracheal Tube of EMG Reinforced NIM Standard and Contact, models 8229306, 8229307, 8229308, || 8229506, 8229507 and 8229508, specific lots.
  • Description du dispositif
    This device is intended for the supervision of surgical procedures for patients who require intraoperative monitoring of nerves, whose nature is non-invasive, assisting the surgeon in the location and mapping of the motor nerves through the use of EMG signals and electrical nerve stimulation. This equipment is accompanied by a series of accessories that connect to the patient in order to carry out the follow-up through the different measurements that the device performs.
  • Manufacturer
    Medtronic Xomed, Inc || Medtronic Xomed Instrumentation S.A.S || Medtronic Xomed Inc. || Fidia Advance Biopolymers S.R.L

Manufacturer

Medtronic Xomed, Inc || Medtronic Xomed Instrumentation S.A.S || Medtronic Xomed Inc. || Fidia Ad...
  • Source
    NIDFSINVIMA