Drug recall D-0276-2015
Product
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
Reason for recall
Subpotent Drug: Heparin raw material was found to have low potency
Lots and codes
Lot #: N003061; N003079; and N003087, Exp 2/29/2016
Recall details
- Recalling firm
- Baxter Healthcare Corp., Deerfield, IL
- Quantity
- 127,746 Viaflex Plus Container
- Distribution
- Nationwide
- Type
- Voluntary: Firm initiated
- Recall initiated
- October 30, 2014
- Terminated
- September 22, 2016
Related products
- Heparin Sodium in Sodium Chloride – drug information
- NDC 0338-0428 Heparin Sodium In Sodium Chloride · Heparin Sodium 200 [USP'U]/100mL · Baxter Healthcare Corporation
- NDC 0338-0431 Heparin Sodium In Sodium Chloride · Heparin Sodium 200 [USP'U]/100mL · Baxter Healthcare Corporation
- NDC 0338-0424 Heparin Sodium In Sodium Chloride · Heparin Sodium 200 [USP'U]/100mL · Baxter Healthcare Corporation
- NDC 0338-0433 Heparin Sodium In Sodium Chloride · Heparin Sodium 200 [USP'U]/100mL · Baxter Healthcare Corporation