FDAMay 14, 2024device

NxStage PureFlow-B Solution, Premixed Dialysate for Hemodialysis, Device Catalog Numbers RFP-400, RFP-401, RFP-402, RFP-403, RFP-404, RFP-405, RFP-406, RFP-453, RFP-454, RFP-456

Official recall recorded by the U.S. Food & Drug Administration.

The hazard

The smaller chamber of the two chamber bag is bursting when nurses are attempting to mix the two chambers prior to use. The electrolyte fluid in the small chamber of the NxStage PureFlow B Solution has a pH of less than 2.0. The solution can be harmful if it comes in contact with the eyes or skin, and/or as a result of a slip or fall injury due to spilled fluid.

What to do

FDA enforcement status: Ongoing

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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