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RECALLED – Hydrocodone bitartrate and acetaminophen 10mg/500 mg tablets | by The U.S. Food and Drug Administration
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RECALLED – Hydrocodone bitartrate and acetaminophen 10mg/500 mg tablets

December 6, 2012 – Product Recall – RECALLED – QUALITEST ISSUES VOLUNTARY, NATIONWIDE RECALL OF 101 LOTS OF HYDROCODONE BITARTRATE and ACETAMINOPHEN TABLETS, USP 10 mg/500 mg DUE TO THE POTENTIAL FOR OVERSIZED TABLETS. For additional information, please refer to the company issued press release available on FDA’s web site at www.fda.gov/Safety/Recalls/ucm331218.htm.

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Taken on December 8, 2012