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NxStage Medical, Inc. recalls NxStage PureFlow-B Solution, Model/Catalog Number: RFP-401, packaged in a case The NxStage PureFLow-B Solution is in
Recalled May 8, 2013 · FDA recall Z-1214-2013 · NxStage Medical
Hazard
Product may be mislabeled. · FDA Class II
Units
1480 cases (2 bags per case)
Sold at
Nationwide Distribution including IL, SC, TX, VA, FL, AR, and NY.
Description
Product may be mislabeled.
Product
NxStage PureFlow-B Solution, Model/Catalog Number: RFP-401, packaged in a case 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 →