DLP®

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
    DMA

14 devices with a similar name

Learn more about the data here

  • Model / Serial
    DLP® Single Stage Venous Cannulae
  • Product Description
    Those cannulae are intended for collection of venous blood from the right side of the heart via the superior or inferior vena cava during cardiopulmonary bypass surgery up to six hours or less.
  • Manufacturer
  • Model / Serial
  • Product Description
    Batch Recall of the Medical Device "DLP Chain of Femoral Artery and DLP® Medium Chambers and Injection Kits"
  • Manufacturer
9 more