Devices

Device Recall NxStage PureFlowB Solution

  • Model / Serial
    F023444
  • Product Classification
    Gastroenterology-Urology Devices
  • Device Class
    2
  • Implanted device?
    No
  • Distribution
    Nationwide Distribution including IL, SC, TX, VA, FL, AR, and NY.
  • Product Description
    NxStage PureFlow-B Solution, Model/Catalog Number: RFP-401, packaged in a case || The NxStage PureFLow-B Solution is indicated for use with renal replacement therapy systems that utilize sterile premixed dialysate during hemodialysis.
  • Manufacturer
    NxStage Medical, Inc.
  • 1 Event

Manufacturer

NxStage Medical, Inc.
  • Manufacturer Address
    NxStage Medical, Inc., 350 Merrimack Street, Lawrence MA 01843-1748
  • Manufacturer Parent Company (2017)
    Nxstage Medical Inc
  • Source
    USFDA

One device with a similar name

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Device Recall NxStage PureFlowB Solution
  • Model / Serial
    Lot Number: F113662
  • Product Classification
    Gastroenterology-Urology Devices
  • Device Class
    2
  • Implanted device?
    No
  • Distribution
    US Distribution including the states of NY, TX, ID, AR, CA and AL
  • Product Description
    NxStage PureFlow-B Solution; Model/Catalog Number: RFP-401. Product is packaged in a case containing two individual 5L bags. || The NxStage PureFlow-B Solution is indicated for use with renal replacement therapy systems that utilize sterile premixed dialysate during hemodialysis.
  • Manufacturer
    NxStage Medical, Inc.