drugs Class II Updated 2014-12-03

Baxter Healthcare Corp. recalls Heparin Sodium in 0.9% Sodium Chloride Injection, 1000 USP H

Recalled 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

Hazard / Issue

Subpotent Drug: Heparin raw material was found to have low potency

Issued by

FDA

Distribution: Nationwide (United States)
Lot/Code Info: Lot #: N003061; N003079; and N003087, Exp 2/29/2016
View official government recall

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