Baxter Healthcare Corp recalls Heparin Sodium and 0.9% Sodium Chloride Injection, 1000 USP Heparin Units, 500 mL in a VIAFLEX Plus Container, Rx Only,
Recalled June 17, 2015 · FDA recall D-1131-2015 · Baxter Healthcare
Hazard
Subpotent Drug; out of specification results for heparin raw material · FDA Class II
Units
145,350 containers
Sold at
Nationwide
Description
Subpotent Drug; out of specification results for heparin raw material
Product
Heparin Sodium and 0.9% Sodium Chloride Injection, 1000 USP Heparin Units, 500 mL in a VIAFLEX Plus Container, Rx Only, Baxter Healthcare Corporation, Deerfield, IL --- NDC 0338-0431-03
Manufacturer(s)
Baxter Healthcare Corp
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →