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

0.9% Sodium Chloride Injection USP MINI-BAG Plus Container, 100 mL VIAFLEX Single Dose…

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 MINI-BAG Plus Container, 100 mL VIAFLEX Single Dose Container bags, Rx only, Baxter Healthcare Corporation, Deerfield, IL 60015 USA, NDC 0338-0553-18, Product Code 2B0043.

Recalling firm
Baxter Healthcare Corp.
NDC code
0338-0553-18
Origin
IL, United States
Initiated by
Voluntary: Firm initiated
FDA recall number
D-1592-2014

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.

Other Chloride recalls

See all