US Drug Recall Register
Class II · Moderate risk Terminated Initiated Jul 6, 2017 (9 years ago)

0.9% Sodium Chloride Injection USP, 250 mL VIAFLEX Container bag, Rx only, Baxter…

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

Why it was recalled

Lack of Assurance of Sterility: Customer complaints for leaking bags.

What was recalled

0.9% Sodium Chloride Injection USP, 250 mL VIAFLEX Container bag, Rx only, Baxter Healthcare Corporation, Deerfield, IL 60015; Distributed in Canada by Baxter Corporation, Toronto, Ontario, Canada, Product Code: 2B1322, NDC 0338-0049-02.

Recalling firm
Baxter Healthcare Corporation
NDC code
0338-0049-02
Origin
IL, United States
Initiated by
Voluntary: Firm initiated
FDA recall number
D-0957-2017

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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