medical Class II Updated 2018-12-05

NxStage Medical, Inc. recalls NxStage PureFlow B Solution-RFP-402, Premixed Dialysate for

Recalled Product

NxStage PureFlow B Solution-RFP-402, Premixed Dialysate for Hemodialysis NxStage PureFlow B Solution is indicated for use with renal replacement therapy systems that utilize sterile premixed dialysate during hemodialysis.

Hazard / Issue

PureFlow B Solution smaller chamber of the two chamber bag can burst electrolyte fluid and cause injury if it comes in contact with the eyes or skin

Issued by

FDA

Distribution: Nationwide (United States)
Lot/Code Info: Lot Numbers: F1708255, F1709285, F1710323, Q1711861, Q1711863, Q1712021, Q1712022, Q1712023, Q1712033, Q1801345, Q1802399, Q1802400
View official government recall

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