Kendall, a division of Tyco Healthcare Group LP

  • 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
  • 2 Events

2 dispositifs dans la base de données

  • Modèle / numéro de série
    Model: 6522, Affected: All Lots beginning with 110000161662 through Lot 15G255462X
  • Modèle / numéro de série
    Model: Product codes: 8888-160325, 8888-160333, 8888-160341, Affected: All lots

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