Update: 1/28/2009 - The U.S Food & Drug Administration in association with ETHEX Corporation has issued another nationwide recall of many products. You can view the full recall list by clicking here.
On November 7, 2008 the U.S. Food & Drug Administration (FDA) in association with ETHEX Corporation issued an urgent nationwide recall of Dextroamphetamine Sulfate Tablets. The Dextroamphetamine Sulfate Tablets been recalled as a precaution, due to the possibility that they may contain oversized tablets. Oversized tablets may contain more than the intended levels of the active drug ingredient, which could result in patients receiving as much as about twice the expected dosage of these drugs.
Dextroamphetamine Sulfate Tablet Recall List
Dextroamphetamine Sulfate Tablets, 10 mg: Lots: 73934, 75892, 77945, 81137, 86320 with expiration dates ranging from 6/2009 to 5/2011
Overdoses of Dextroamphetamine Sulfate Tablets can have serious, life-threatening consequences. In the case of Dextroamphetamine Sulfate, these consequences can include rapid heart rate and high blood pressure.
Do I Have a Dextroamphetamine Sulfate Tablet Recall Lawsuit?
If you or a loved one have experienced a serious side effect related to the recall of Dextroamphetamine Sulfate Tablets, you should contact us immediately. You may be entitled to compensation for your injuries and we can help. Please use the form below for a free case evaluation.
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