E-Z-HD (Barium Sulfate for Oral Suspension), 98% w/w, 340 g bottle, Rx only, MFG: Bracco Diagnostics Inc., NDC 32909-764-01
Reason cGMP deviations: Temperature abuse
Class II — Moderate risk. May cause temporary or reversible harm; serious harm unlikely.
Failed stability specifications: Out-of-specification (OOS) result for a preservative assay - methylparaben - during stability testing of one lot.
E-Z-Paste Barium Sulfate Esophageal Cream (60% w/w), 454 g tube, Rx only, Manufactured by E-Z-EM Canada Inc. for E-Z-EM Inc. a subsidiary of Bracco Diagnostics Inc., Monroe Twp., NJ 0883, NDC 32909-770-01
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.
Reason cGMP deviations: Temperature abuse
Reason Failed stability specifications:This recall has been initiated due to out of specification results for viscosity.
Reason Subpotent Drug: Low out of specification results for both pH and assay obtained during routine stability testing after 36 months.
Reason Failed Stability Testing: This product is below specification for preservative content.
Reason Failed Stability Specifications: Tagitol V Barium Sulfate Lot #65846 sampled at 10 months exhibited results above the upper specification for…
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