US Drug Recall Register
Class I · High risk Terminated Initiated Jan 21, 2016 (11 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: identified as cardboard.

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, Product Code 2B0043, NDC 0338-0553-18.

Recalling firm
Baxter Healthcare Corp.
NDC code
0338-0553-18
Origin
IL, United States
Initiated by
Voluntary: Firm initiated
FDA recall number
D-0862-2016

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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