N'VISION APPLICATION CARD

Manufacturer

  • Manufacturer Address
    BRAMPTON
  • Manufacturer Parent Company (2017)
  • Manufacturer comment
    “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

3 devices with a similar name

Learn more about the data here

  • Model / Serial
    Model Catalog: 8870 (Lot serial: All Lots)
  • Product Description
    RESTOREADVANCED MULTI-PROGRAM NEUROSTIMULATOR - N'VISION APPLICATION CARD;ACTIVA RC NEUROSTIMULATOR - N'VISION APPLICATION CARD;RESTOREULTRA MULTI-PROGRAM NEUROSTIMULATOR SYST - N'VISION APPLICATION CARD;ACTIVA PC INS - N'VISION APPLICATION CARD;N'VISION
  • Manufacturer
  • Model / Serial
    Model Catalog: 8870 (Lot serial: Recall is not lot specific)
  • Product Description
    N'VISION APPLICATION CARD
  • Manufacturer
  • Model / Serial
    Model Catalog: 8870 (Lot serial: Not Applicable)
  • Product Description
    N'VISION APPLICATION CARD
  • Manufacturer