Device Recall Deltec ProPort

  • Model / Serial
    Lot M27048
  • Product Classification
  • Device Class
    2
  • Implanted device?
    Yes
  • Distribution
    The recalled products were shipped nationwide in the United States and worldwide.
  • Product Description
    ProPort Low Profile Plastic Venous Access System, with PolyFlow Polyurethane Catheter, 1.9mm O.D. x 1.0mm I.D., 6 French Introducer Set, REF 21-4183-24
  • Manufacturer
  • 1 Event

Manufacturer

  • Manufacturer Address
    Deltec, Inc, 1265 Grey Fox Rd, Saint Paul MN 55112-6929
  • Source
    USFDA

3 devices with a similar name

Learn more about the data here

  • Model / Serial
    Lot M27054
  • Product Classification
  • Device Class
    2
  • Implanted device?
    Yes
  • Distribution
    The recalled products were shipped nationwide in the United States and worldwide.
  • Product Description
    ProPort Plastic Venous Access System, with PolyFlow Polyurethane Catheter, 2.6mm O.D. x 1.6mm I.D., 8.5 French Introducer Set, REF 21-4155-24
  • Manufacturer
  • Model / Serial
    Lot M27136
  • Product Classification
  • Device Class
    2
  • Implanted device?
    Yes
  • Distribution
    The recalled products were shipped nationwide in the United States and worldwide.
  • Product Description
    ProPort Plastic Venous Access System, Pre-assembled with PolyFlow Polyurethane Catheter, 2.6mm O.D. x 1.6mm I.D., 8.5 French Introducer Set, REF 21-4165-24
  • Manufacturer
  • Model / Serial
    Lot M27046
  • Product Classification
  • Device Class
    2
  • Implanted device?
    Yes
  • Distribution
    The recalled products were shipped nationwide in the United States and worldwide.
  • Product Description
    ProPort Low Profile Plastic Venous Access System, with PolyFlow Polyurethane Catheter, 2.6mm O.D. x 1.6mm I.D., 8.5 French Introducer Set, REF 21-4171-24
  • Manufacturer