Devices

Device Recall Phoenix Monitor

  • Model / Serial
    Product code: 6997274; Lot codes: 160718E, 160720E, 160825E
  • Product Classification
    Gastroenterology-Urology Devices
  • Device Class
    2
  • Implanted device?
    No
  • Distribution
    Nationwide Distribution
  • Product Description
    Maintenance Kit PH2, Cod. 6997274 || The Phoenix Hemodialysis delivery system is intended to be used to provide high flux and low flux hemodialysis, hemofiltration and ultrafiltration on patients weighing 15 Kilograms or more. The Phoenix system is to be used with either high or low permeability dialyzers. The device is intended to be used by trained operators when prescribed by a physician, in a chronic care dialysis facility or acute care unit
  • Manufacturer
    Baxter Healthcare Corporation
  • 1 Event

Manufacturer

Baxter Healthcare Corporation
  • Manufacturer Address
    Baxter Healthcare Corporation, 1 Baxter Pkwy, Deerfield IL 60015-4625
  • Manufacturer Parent Company (2017)
    Baxter International
  • Source
    USFDA

One device with a similar name

Learn more about the data here

Device Recall Phoenix Monitor
  • Model / Serial
    Product code: 6997266; Lot codes: 1607250, 160824D, 161005D, 161026D
  • Product Classification
    Gastroenterology-Urology Devices
  • Device Class
    2
  • Implanted device?
    No
  • Distribution
    Nationwide Distribution
  • Product Description
    Maintenance Kit PH1, Cod. 6997266 || The Phoenix Hemodialysis delivery system is intended to be used to provide high flux and low flux hemodialysis, hemofiltration and ultrafiltration on patients weighing 15 Kilograms or more. The Phoenix system is to be used with either high or low permeability dialyzers. The device is intended to be used by trained operators when prescribed by a physician, in a chronic care dialysis facility or acute care unit
  • Manufacturer
    Baxter Healthcare Corporation