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Recall Observatory FDA recall evidence

Device 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.

Z-1706-2019

April 11, 2019

Class II

Product summary

Firm
NxStage Medical, Inc.
Event
Event 82693
Status
Terminated
Classification
Class II
Quantity
1998 units
Official record key
device-enforcement:Z-1706-2019

Official wording

Reason: Certain lots were mislabeled with incorrect product number.

Code information: Lot Number: Q1811792 Exp Date: 11/1/2020

Distribution pattern: US Nationwide Distribution - AZ, CA, DC, FL, GA, IL, IN, MI, NC, NH, NV, PA, TX & VA

Derived failure modes

  • Labeling or packaging

    reason.labeling_packaging · v1.0.0

    mislabeled