US Drug Recall Register
Class II · Moderate risk Terminated Initiated Jul 2, 2015 (11 years ago)

0.9% Sodium Chloride Injection USP, 500 mL in VIAFLEX Plastic Container, Baxter…

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

Why it was recalled

Presence of Particulate Matter and Lack of Assurance of Sterility: The firm received a complaint for customer of presence of particulate matter, leaky containers, and missing port protectors.

What was recalled

0.9% Sodium Chloride Injection USP, 500 mL in VIAFLEX Plastic Container, Baxter Healthcare Corporation Deerfield, IL 60015, NDC 0338-0049-03.

Recalling firm
Baxter Healthcare Corp.
NDC code
0338-0049-03
Origin
IL, United States
Initiated by
Voluntary: Firm initiated
FDA recall number
D-1326-2015

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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