US Drug Recall Register
Class II · Moderate risk Terminated Initiated Jun 3, 2015 (11 years ago)

Heparin Sodium and 0.9% Sodium Chloride Injection, 1000 USP Heparin Units, 500 mL in a…

Class II — Moderate risk. May cause temporary or reversible harm; serious harm unlikely.

Why it was recalled

Subpotent Drug; out of specification results for heparin raw material

What 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

Recalling firm
Baxter Healthcare Corp
NDC code
0338-0431-03
Origin
IL, United States
Initiated by
Voluntary: Firm initiated
FDA recall number
D-1131-2015

What should you do? A recall doesn't always mean your specific bottle is affected - it often applies to certain lots only. Check the lot number on your package against the FDA notice, and talk to your pharmacist before stopping any medication.

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