medical Class II Updated 2018-12-05

NxStage Medical, Inc. recalls NxStage PureFlow B Solution-RFP-RFP-456, Premixed Dialysate

Recalled Product

NxStage PureFlow B Solution-RFP-RFP-456, 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: F1708258, F1710322, Q1711910, Q1711911, Q1712093, Q1801227, Q1801342, Q1801343, Q1802393, Q1803816
View official government recall

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