MAXIMA CARMEDA BONDED VENOUS RESERVOIR

  • Modèle / numéro de série
    Model Catalog: MVR-800 (Lot serial: 9908001526 9909002808); Model Catalog: CBMVR800 (Lot serial: 9910004162.); Model Catalog: MVR-800 (Lot serial: 9910004162.); Model Catalog: CBMVR800 (Lot serial: 0001004908 0001001002); Model Catalog: CBMVR800 (Lot serial: 9908001526 9909002808); Model Catalog: MVR-800 (Lot serial: 0007001067 0008002729); Model Catalog: MVR-800 (Lot serial: 0001004908 0001001002); Model Catalog: CBMVR800 (Lot serial: 0003003002 0004003693); Model Catalog: MVR-800 (Lot serial: 0003003002 0004003693); Model Catalog: CBMVR800 (Lot serial: 0007001067 0008002729)
  • Description du dispositif
    MEDTRONIC VENOUS RESERVOIR (MVR)
  • Manufacturer
  • 1 Event

Fabricant

  • Adresse du fabricant
    BRAMPTON
  • Société-mère du fabricant (2017)
  • Commentaire du fabricant
    “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