PlainRecalls
FDA Drug Moderate Class II Terminated

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.