FDAFDA · Food and drugs·Recall number D-0276-2015
Heparin Sodium in 0.9% Sodium Chloride Injection, 1000 USP Heparin Units, 500 mL in a VIAFLEX Plus Container, Rx only, Manufactured for Baxter Healthcare Corporation, One Baxter Parkway, Deerfield, IL 60015 by Baxter Healthcare Corporation 250 Road 144 Jayuya, Puerto Rico, 00664, NDC 0338-0431-03
Published December 3, 2014 · Recall initiated: October 30, 2014
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
Subpotent Drug: Heparin raw material was found to have low potency
What to do
Voluntary: Firm initiated · Letter
Recall details
- Brand
- HEPARIN SODIUM IN SODIUM CHLORIDE
- Manufacturer
- Baxter Healthcare Corp.
- Distributor
- Nationwide
- Lot
- Lot #: N003061; N003079; and N003087, Exp 2/29/2016
- Risk classification
- Class II
- Area (FDA)
- drug
- Country
- United States
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