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NxStage Medical, Inc. recalls NxStage PureFlow-B Solution; Model/Catalog Number: RFP-401. Product is packaged in a case containing two individual 5L
Recalled March 5, 2014 · FDA recall Z-1073-2014 · NxStage Medical
Hazard
Mislabeled product. · FDA Class II
Units
969 cases (2 bags per case)
Sold at
US Distribution including the states of NY, TX, ID, AR, CA and AL
Description
Mislabeled product.
Product
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(s)
NxStage Medical, Inc.
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →