US Drug Recall Register
Class III · Low risk Terminated Initiated May 27, 2015 (11 years ago)

E-Z-CAT Dry Barium Sulfate for Suspension (2% w/w after mixing), 23 g foil pouches, Rx…

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

Why it was recalled

Failed stability specifications:This recall has been initiated due to out of specification results for viscosity.

What was recalled

E-Z-CAT Dry Barium Sulfate for Suspension (2% w/w after mixing), 23 g foil pouches, Rx only, Manufactured by E-Z-EM Canada Inc. a subsidiary of E-Z-EM Inc., Lake Success NY NDC 32909-727-01

Recalling firm
Bracco Diagnostic Inc
NDC code
32909-727-01
Origin
NJ, United States
Initiated by
Voluntary: Firm initiated
FDA recall number
D-1147-2015

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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