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NxStage Medical, Inc. recalls NxStage PureFlow B Solution, REF RFP-400, M535RFP4000 Product NxStage PureFlow B Solution is indicated for use with r
Recalled June 12, 2019 · FDA recall Z-1706-2019 · NxStage Medical
Hazard
Certain lots were mislabeled with incorrect product number. · FDA Class II
Units
1998 units
Sold at
US Nationwide Distribution - AZ, CA, DC, FL, GA, IL, IN, MI, NC, NH, NV, PA, TX & VA
Description
Certain lots were mislabeled with incorrect product number.
Product
NxStage PureFlow B Solution, REF RFP-400, M535RFP4000 Product 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 →