FDA recall record

Bracco Diagnostic E-Z-CAT Dry Barium Sulfate for Suspension (2% w/w after mixing), 23 g foil recall — FDA D-1147-2015

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

Class IIIclassification
D-1147-2015official record ID
Jul 1, 2015report date

Recall record at a glance

Official recordD-1147-2015
CategoryDrug Recalls
ClassificationClass III
FDA record statusTerminated
Recalling firmBracco Diagnostic Inc.
Report dateJul 1, 2015
Recall initiation dateMay 27, 2015
Quantity1008 boxes
LocationMonroe Township, NJ, United States

Official product description

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

Why the product was recalled

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

Distribution information

Nationwide

How to read the classification

FDA Class III generally covers situations in which use of or exposure to the product is not likely to cause adverse health consequences. The classification displayed here is taken from the FDA enforcement record.

Additional record details

Recall type: Voluntary: Firm initiated. Initial notification: Letter.

What to do next

If you believe you have the recalled product, use the recall number and firm information above to confirm the official notice and follow the instructions issued by the FDA, recalling firm, retailer or product manufacturer. For drugs and medical devices, decisions about treatment or medical care should be discussed with a qualified health professional.

About this record

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