Concerto

Manufacturer

  • 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
    SATP

29 devices with a similar name

Learn more about the data here

  • Model / Serial
    Model: , Affected:
  • Manufacturer
  • Model / Serial
    Model: , Affected: batch of devices manufactured between 7th March 2014 and 20th April 2015.
  • Manufacturer
  • Model / Serial
  • Product Description
    medical_device
  • Manufacturer
  • Model / Serial
    Lots 7575613, 7583594, 7715339 and 7730068.
  • Product Classification
  • Device Class
    2
  • Implanted device?
    No
  • Distribution
    Nationwide, Germany, Italy, Netherlands, Spain and Sweden.
  • Product Description
    Boston Scientific brand Concerto Bipolar Needle Electrode, sterile, latex free, Model M001262400, catalog number 26-240.
  • Manufacturer
24 more