FDA recall record

E-Z-HD (barium sulfate) For Suspension (98% w/w), 340 g bottle recall — FDA D-1536-2014

Subpotent Drug: Low out of specification results for both pH and assay obtained during routine stability testing after 36 months.

Class IIIclassification
D-1536-2014official record ID
Aug 20, 2014report date

Recall record at a glance

Official recordD-1536-2014
CategoryDrug Recalls
ClassificationClass III
FDA record statusTerminated
Recalling firmBracco Diagnostic Inc.
Report dateAug 20, 2014
Recall initiation dateJul 2, 2014
Quantity216,792 bottles
LocationMonroe Township, NJ, United States

Official product description

E-Z-HD (barium sulfate) For Suspension (98% w/w), 340 g bottle, Rx Only, Manufactured by E-Z-EM Canada Inc., a subsidiary of E-Z-EM, Inc., Lake Success, NY 11042, NDC 32909-764-01.

Why the product was recalled

Subpotent Drug: Low out of specification results for both pH and assay obtained during routine stability testing after 36 months.

Distribution information

Nationwide and 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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