FDAOctober 17, 2018device
NxStage PureFlow B Solution-RFP-RFP-454, Premixed Dialysate for Hemodialysis NxStage PureFlow B Solution is indicated for use with renal replacement therapy systems that utilize sterile premixed dialysate during hemodialysis.
Official recall recorded by the U.S. Food & Drug Administration.
The hazard
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
What to do
FDA enforcement status: Terminated
Brands named
nxstage medicalnxstage
Recall history
Other federal recalls tied to the same brand — a factual pattern, straight from the source data.
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