Events

Rappel de DEVON BIRTHDAY KIT C-SECTION BASIC

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

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
    53127
  • Classe de risque de l'événement
    II
  • Date de mise en oeuvre de l'événement
    2016-12-29
  • 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
    Customers have reported that on rare occasion the devon light glove may split upon application to the devon light handle adapter. some of the reported splits resulted from difficult application of the light glove to the handle adapter. more recently clinicians have reported finding splits in the light glove following surgery completion where no difficulty in application of the light glove was encountered or finding splits directly out of the package. a split in the light glove causes a breach in the sterile field and can increase the potential for infection. medtronic has received notice of two patient adverse events (infection) in which light glove splits were found at the conclusion of surgery.

Device

DEVON BIRTHDAY KIT C-SECTION BASIC
  • Modèle / numéro de série
    Model Catalog: 31404851 (Lot serial: All lots with 630xxx and lower); Model Catalog: 50000148 (Lot serial: All lots with 630xxx and lower); Model Catalog: 31141552 (Lot serial: All lots with 630xxx and lower); Model Catalog: 31140216 (Lot serial: All lots with 630xxx and lower); Model Catalog: 31140257 (Lot serial: All lots with 630xxx and lower); Model Catalog: 31140208 (Lot serial: All lots with 630xxx and lower)
  • Description du dispositif
    DEVON BIRTHDAY KIT C-SECTION BASIC;DEVON OR MINI KIT;DEVON LIGHT GLOVE
  • Manufacturer
    COVIDIEN

Manufacturer

COVIDIEN
  • Adresse du fabricant
    SAINT-LAURENT
  • 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