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
Reported: December 3, 2014 Initiated: October 30, 2014 #D-0276-2015
Product Description
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
Details
- Recalling Firm
- Baxter Healthcare Corp.
- Units Affected
- 127,746 Viaflex Plus Container
- Distribution
- Nationwide
- Location
- Deerfield, IL
Frequently Asked Questions
What product was recalled? ▼
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. Recalled by Baxter Healthcare Corp.. Units affected: 127,746 Viaflex Plus Container.
Why was this product recalled? ▼
Subpotent Drug: Heparin raw material was found to have low potency
Which agency issued this recall? ▼
This recall was issued by the FDA Drug on December 3, 2014. Severity: Moderate. Recall number: D-0276-2015.
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