Events

Rappel de EON MINI NEUROSTIMULATION SYSTEM - IMPLANTABLE PULSE GENERATOR

Selon Health Canada (via FOI), ce/cet/cette rappel concerne un dispositif en/au/aux/à Canada qui a été fabriqué par ABBOTT MEDICAL CANADA INC..

Qu'est-ce que c'est?

Une correction ou un retrait opéré par un fabricant afin de répondre à un problème causé par un dispositif médical. Les rappels surviennent lorsqu'un dispositif médical est défectueux, lorsqu'il pourrait poser un risque pour la santé, ou les deux à la fois.

En savoir plus sur les données ici
  • Type d'événement
    Recall
  • ID de l'événement
    24582
  • Classe de risque de l'événement
    II
  • Date de mise en oeuvre de l'événement
    2012-07-27
  • Pays de l'événement
    Canada
  • Source de l'événement
    HC
  • Notes / Alertes
    Canadian data is current through March 2018. All of the data comes from Health Canada, 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 Canada.
  • Notes supplémentaires dans les données
  • Cause
    Product investigation and analysis concerning reports of the inability to communicate or recharge the eon mini ipg has identified weld cracks in the ipg's inner battery as the cause of this issue. there is a need to more frequently maintain and replace welding fixtures to assure complete alignment between the welding apparatus and the battery. there is no exposure of electrolyte material to the patient.

Device

EON MINI NEUROSTIMULATION SYSTEM - IMPLANTABLE PULSE GENERATOR
  • Modèle / numéro de série
    Model Catalog: 3788 (Lot serial: 13709418 13710437 13725081); Model Catalog: 3788 (Lot serial: 13691790 13691827 13691967); Model Catalog: 3788 (Lot serial: 13691341 13648229 13691401); Model Catalog: 3788 (Lot serial: SERIAL NUMBERS:13548109); Model Catalog: 3788 (Lot serial: 13691522 13672787 13691786); Model Catalog: 3788 (Lot serial: 13656051 13672978 13673518); Model Catalog: 3788 (Lot serial: 13709498 13523004 13545855)
  • Description du dispositif
    EON MINI NEUROSTIMULATION SYSTEM-IMPLANTABLE PULSE GENERATOR
  • Manufacturer
    ABBOTT MEDICAL CANADA INC.

Manufacturer

ABBOTT MEDICAL CANADA INC.
  • Adresse du fabricant
    MISSISSAUGA
  • Société-mère du fabricant (2017)
    Abbott Laboratories
  • Commentaire du fabricant
    “We are in constant communication with regulatory agencies and competent authorities worldwide which allows us to implement global recalls or in-country communication quickly and effectively,” Abbott, which now owns St. Jude Medical told ICIJ in a statement. In addition to sending global notices to physicians worldwide, we also make sure that product advisories are available online and classification of product recalls and product advisories are determined by global regulatory bodies which can impact the timing in any given country. MD companies follow varying regulations in different countries. In come countries software is not regulated so a recall in one country related to software would not be classified as a recall or field action in another. In addition, review cycles within the regulatory process can be different in each country which can impact communication and recall timing.
  • Source
    HC