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.
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