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RECALLED - Bracco Diagnostics Isovue | by The U.S. Food and Drug Administration
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RECALLED - Bracco Diagnostics Isovue

November 27, 2012 – Product Recall – Bracco Diagnostics Inc. Issues Voluntary Nationwide Recall of Isovue® (iopamidol injection) Pre-Filled Power Injector Syringes due to Presence of Particulates. For additional information, please refer to the company issued press release available on FDA’s web site at www.fda.gov/Safety/Recalls/ucm329740

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Taken on November 29, 2012