Devon Light Glove

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
    SMPA

92 devices with a similar name

Learn more about the data here

  • Model / Serial
    Model: Item Numbers: 571711, 31140208, 31140216, 31140257, Affected: Lot numbers 508xxx or lower
  • Manufacturer
  • Model / Serial
    Model: 2900456-0x, 2900846-0x, 2901816-0x, 2902500-0x, 2903916-0x, 2904409-0x, 2906757-00, 2908159-0x, 2908973-0x, Affected: All lot numbers ending xx2, xx3, xx4, and lot numbers 015, 025, 035, and 045 delivered before 6 May 2015
  • Manufacturer
  • Model / Serial
    Model: 471711 31140208 31140216 and 31140257, Affected:
  • Manufacturer
  • Model / Serial
  • Product Description
    medical_device
  • Manufacturer
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