US Drug Recall Register
Class III · Low risk Terminated Initiated Dec 16, 2013 (13 years ago)

VoLumen Barium Sulfate Suspension (0.1 % w/v, 0.1 ww/w), 450 mL bottle, Rx Only…

Class III — Low risk. Unlikely to cause harm, but violates FDA regulations.

Why it was recalled

Failed Stability Testing: This product is below specification for preservative content.

What was recalled

VoLumen Barium Sulfate Suspension (0.1 % w/v, 0.1 ww/w), 450 mL bottle, Rx Only. Manufactured by E-Z-EM Canada Inc. a subsidiary or E-Z-EM, Inc. Lake Success, NY 11042. NDC 32909-945-03.

Recalling firm
Bracco Diagnostics Inc
NDC code
32909-945-03
Origin
NJ, United States
Initiated by
Voluntary: Firm initiated
FDA recall number
D-1083-2014

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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