PlainRecalls
FDA Drug Moderate Class II Terminated

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

Reported: June 17, 2015 Initiated: June 3, 2015 #D-1131-2015

Product Description

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

Reason for Recall

Subpotent Drug; out of specification results for heparin raw material

Details

Recalling Firm
Baxter Healthcare Corp
Units Affected
145,350 containers
Distribution
Nationwide
Location
Deerfield, IL

Frequently Asked Questions

What product was recalled?
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. Recalled by Baxter Healthcare Corp. Units affected: 145,350 containers.
Why was this product recalled?
Subpotent Drug; out of specification results for heparin raw material
Which agency issued this recall?
This recall was issued by the FDA Drug on June 17, 2015. Severity: Moderate. Recall number: D-1131-2015.