DLP Single Stage Venous Cannula with Metal Tip

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

4 devices with a similar name

Learn more about the data here

  • Model / Serial
    Model: 67318 and 69328, Affected: 2012110851, 2012121004 and 2012121364
  • Manufacturer
  • Model / Serial
  • Product Description
    Injections / Infusions / Transfusions / Dialysis - catheters
  • Manufacturer
  • Model / Serial
  • Product Description
    DLP Single Stage Venous Cannula with Metal Tip
  • Manufacturer
  • Model / Serial
    DLP Single Stage Venous Cannula with Metal Tip (Intended for the collection of deoxygenated blood from the superior and/or inferior vena cava during cardiopulmonary bypass)Model Numbers: 69324, 69328, 69331Lot Numbers: 2012121362, 2012121364, 2012121005 and 2012121063ARTG Number: 155002
  • Product Classification
  • Manufacturer