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 Isosorbide Mononitrate Extended Release Tablets. The Isosorbide Mononitrate Extended Release 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.
Isosorbide Mononitrate Extended Release Tablet Recall List
Isosorbide Mononitrate Extended Release Tablets, 30 mg: Lots: 62355, 66423, and 68102 with expiration dates ranging from 11/2008 to 8/2009
Isosorbide Mononitrate Extended Release Tablets, 60 mg: Lots: 63466, 66034, 67351, and 67354 with expiration dates ranging from 12/2008 to 11/2009
Overdoses of Isosorbide Mononitrate Extended Release Tablets can have serious, life-threatening consequences. In the case of Isosorbide Mononitrate, these consequences can include fainting and low blood pressure.
Do I Have an Isosorbide Mononitrate Extended Release Tablet Recall Lawsuit?
If you or a loved one have experienced a serious side effect related to the recall of Isosorbide Mononitrate Extended Release 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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