US Drug Recall Register
Class II · Moderate risk Terminated Initiated Sep 6, 2018 (8 years ago)

0.9% Sodium Chloride Injection USP 50 mL Viaflex container Baxter Healthcare Corporation…

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

Why it was recalled

cGMP Deviation

What was recalled

0.9% Sodium Chloride Injection USP 50 mL Viaflex container Baxter Healthcare Corporation Deerfield, IL 60015 -- NDC 0338-0049-31

Recalling firm
Baxter Healthcare Corporation
NDC code
0338-0049-31
Origin
IL, United States
Initiated by
Voluntary: Firm initiated
FDA recall number
D-1190-2018

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.

Other Chloride recalls

See all