FDAFDA · Food and drugs·Recall number D-1131-2015
Heparin Sodium and 0.9% Sodium Chloride Injection, 1000 USP Heparin Units, 500 mL in a VIAFLEX Plus Container, Rx Only, Baxter Healthcare Corporation, Deerfield, IL --- NDC 0338-0431-03
Published June 17, 2015 · Recall initiated: June 3, 2015
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; out of specification results for heparin raw material
What to do
Voluntary: Firm initiated · Letter
Recall details
- Brand
- HEPARIN SODIUM IN SODIUM CHLORIDE
- Manufacturer
- Baxter Healthcare Corp
- Distributor
- Nationwide
- Lot
- Product Code: 280953 Lots: N002998 and N003004 exp 12/31/15; and lot N003038 exp. 01/31/2016
- Risk classification
- Class II
- Area (FDA)
- drug
- Country
- United States
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