Baxter Healthcare Corp. recalls Heparin Sodium in 0.9% Sodium Chloride Injection, 1000 USP Heparin Units, 500 mL in a VIAFLEX Plus Container, Rx only, M
Recalled December 3, 2014 · FDA recall D-0276-2015 · Baxter Healthcare
Hazard
Subpotent Drug: Heparin raw material was found to have low potency · FDA Class II
Units
127,746 Viaflex Plus Container
Sold at
Nationwide
Description
Subpotent Drug: Heparin raw material was found to have low potency
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
Manufacturer(s)
Baxter Healthcare Corp.
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →