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

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
  • ID de l'événement
  • Classe de risque de l'événement
  • Date de mise en oeuvre de l'événement
  • Pays de l'événement
  • Source de l'événement
  • 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
    Due to a time conversion error data uploaded from the iprot2 recorder to the carelink ipro software using the new carelink ipro uploader feature may result in incorrect reports. this pertains only to reports generated between september 23 2017 and september 27 2017 that used the new carelink ipro uploader feature. specifically when data from the ipro2 recorder was uploaded using the new carelink ipro uploader feature the glucose reading timestamps inadvertently defaulted to greenwich mean time (gmt) /coordinated universal time (utc). manufacturer determined that the difference in time zones could result in calculation and display errors on the reports. this could lead to potential differences or inaccuracies in the sensor tracings which also affect the display of meals and activities and the resulting report.


  • Modèle / numéro de série
    Model Catalog: MMT-7340 (Lot serial: 3081022); Model Catalog: MMT-7340 (Lot serial: 3087942); Model Catalog: MMT-7340 (Lot serial: 3030864); Model Catalog: MMT-7340 (Lot serial: 3088217); Model Catalog: MMT-7340 (Lot serial: 3075370); Model Catalog: MMT-7340 (Lot serial: 3058602); Model Catalog: MMT-7340 (Lot serial: 3088123)
  • Description du dispositif
  • Manufacturer


  • Adresse du fabricant
  • Société-mère du fabricant (2017)
  • Commentaire du fabricant
    “If our surveillance systems identify a potential performance issue, our personnel promptly evaluate the problem, including, when appropriate, conducting root cause investigations and internal testing to assess whether the product continues to meet specifications and defined performance criteria,” Medtronic told ICIJ in a statement. “In some cases, based on this evaluation, Medtronic may determine that a recall is necessary.” The company said that it communicates with healthcare providers and/or patients and provide recommendations to address such issues. Medtronic noted that these communications can include letters, emails, calls, press releases, physician notifications and social media postings, as well as informing the FDA and other regulators of the actions.
  • Source