US Drug Recall Register
Class II · Moderate risk Terminated Initiated Jun 21, 2013 (13 years ago)

Gastrografin (Diatrizoate Meglumine and Diatrizoate Sodium Solution), USP, 37%…

Class II — Moderate risk. May cause temporary or reversible harm; serious harm unlikely.

Why it was recalled

Presence of foreign substance: One lot of the product may contain black foreign particles

What was recalled

Gastrografin (Diatrizoate Meglumine and Diatrizoate Sodium Solution), USP, 37% Organically Bound Iodine, 120 ml bottle, Rx only, Manufactured for Bracco Diagnostics Inc. Princeton, NJ 08543 by Therapex, Division of E-Z-EM Canada Inc. Anjou Quebec H1J2Z4, Canada, NDC 0270-0445-40

Recalling firm
Bracco Diagnostics Inc
NDC code
0270-0445-40
Origin
NJ, United States
Initiated by
Voluntary: Firm initiated
FDA recall number
D-885-2013

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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