US Drug Recall Register
Class II · Moderate risk Terminated Initiated Mar 23, 2015 (11 years ago)

0.9% Sodium Chloride Injection, USP, 50 mL, VIAFLEX Plastic Container Multi Pack, Rx…

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

Why it was recalled

Lack of Assurance of Sterility; increased complaints received for leaks

What was recalled

0.9% Sodium Chloride Injection, USP, 50 mL, VIAFLEX Plastic Container Multi Pack, Rx Only, Baxter Healthcare Corporation, Deerfield, IL , Product code 2B1308, NDC 0338-0049-31

Recalling firm
Baxter Healthcare Corp
NDC code
0338-0049-31
Origin
IL, United States
Initiated by
Voluntary: Firm initiated
FDA recall number
D-0429-2015

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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