US Drug Recall Register
Class I · High risk Terminated Initiated Jul 11, 2014 (12 years ago)

0.9% Sodium Chloride Injection USP, packaged in a) 50 mL VIAFLEX Container bags, NDC…

Class I — High risk. Reasonable probability of serious harm or death.

Why it was recalled

Presence of Particulate Matter: particulate matter identified as fibers and/or plastics.

What was recalled

0.9% Sodium Chloride Injection USP, packaged in a) 50 mL VIAFLEX Container bags, NDC 0338-0049-41, Product Code 2B1306; and b) 100 mL VIAFLEX Container bags, NDC 0338-0049-18, Product Code 2B1302, Rx only, Baxter Healthcare Corporation, Deerfield, IL 60015 USA.

Recalling firm
Baxter Healthcare Corp.
NDC code
0338-0049-41
Origin
IL, United States
Initiated by
Voluntary: Firm initiated
FDA recall number
D-1591-2014

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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