Events

Rappel de DLP SINGLE STAGE VENOUS RETURN CANNULAE

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
    Recall
  • ID de l'événement
    31355
  • Classe de risque de l'événement
    II
  • Date de mise en oeuvre de l'événement
    2011-12-14
  • 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
    The purpose of this field action is to inform affected customers that the instructions for use for the dlp single stage venous cannulae are in the process of being updated. the current precaution statement found below referencing ventricular assist procedures will be identified as a contraindication in the updated instructions for use: do not use this product for extended terms such as ventricular assist procedures.

Device

DLP SINGLE STAGE VENOUS RETURN CANNULAE
  • Modèle / numéro de série
    Model Catalog: 68140 (Lot serial: >100 numbers contact mfg); Model Catalog: 68136 (Lot serial: >100 numbers contact mfg); Model Catalog: 68138 (Lot serial: >100 numbers contact mfg); Model Catalog: 68134 (Lot serial: >100 numbers contact mfg); Model Catalog: 68132 (Lot serial: >100 numbers contact mfg); Model Catalog: 68130 (Lot serial: >100 numbers contact mfg); Model Catalog: 68128 (Lot serial: >100 numbers contact mfg); Model Catalog: 68126 (Lot serial: >100 numbers contact mfg); Model Catalog: 68124 (Lot serial: >100 numbers contact mfg); Model Catalog: 68122 (Lot serial: >100 numbers contact mfg); Model Catalog: 68120 (Lot serial: >100 numbers contact mfg); Model Catalog: 68118 (Lot serial: >100 numbers contact mfg); Model Catalog: 68116 (Lot serial: >100 numbers contact mfg); Model Catalog: 68114 (Lot serial: >100 numbers contact mfg); Model Catalog: 68112 (Lot serial: >100 numbers contact mfg); Model Catalog: 67640 (Lot serial: >100 numbers contact mfg); Model Catalog: 67636 (Lot serial: >100 numbers
  • Description du dispositif
    DLP Single Stage Metal Tip Venous Cannula
  • Manufacturer
    MEDTRONIC OF CANADA LTD.

Manufacturer

MEDTRONIC OF CANADA LTD.
  • Adresse du fabricant
    BRAMPTON
  • Société-mère du fabricant (2017)
    Medtronic plc
  • 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
    HC