FDAFDA · Food and drugs·Recall number Z-1214-2013
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.
Published May 8, 2013 · Recall initiated: March 18, 2013
Status when published: Terminated — openFDA updates weekly, so this field may not reflect the current status. Always confirm with the official notice.
What's the hazard
Product may be mislabeled.
What to do
Voluntary: Firm initiated · E-Mail
Recall details
- Manufacturer
- NxStage Medical, Inc.
- Distributor
- Nationwide Distribution including IL, SC, TX, VA, FL, AR, and NY.
- Lot
- F023444
- Risk classification
- Class II
- Area (FDA)
- device
- Country
- United States
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