FDA recall record

Bracco Diagnostics VoLumen Barium Sulfate Suspension (0.1 % w/v, 0.1 ww/w), 450 mL bottle recall — FDA D-1083-2014

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

Class IIIclassification
D-1083-2014official record ID
Feb 19, 2014report date

Recall record at a glance

Official recordD-1083-2014
CategoryDrug Recalls
ClassificationClass III
FDA record statusTerminated
Recalling firmBracco Diagnostics Inc.
Report dateFeb 19, 2014
Recall initiation dateDec 16, 2013
Quantity54,648 bottles
LocationMonroe Township, NJ, United States

Official product description

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.

Why the product was recalled

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

Distribution information

Nationwide including Puerto Rico

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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