Actavis Totowa LLC recalled all lots of Digitek for oral use in April of 2008. The product was recalled because of the possibility that the tablets, which are double appropriate thickness and containing twice the active ingredient, may have been commercially released.
If you or your loved ones have been injured by Digitek tablets, you should contact an attorney immediately. You or our loved ones may be entitled to compensation for your injuries.
Digitek tablets that are twice the thickness appropriate may have been commercially released. These tablets contain twice the amount of the active ingredient in Digitek making them dangerous to patients with renal failure. These patients may develop digitalis toxicity. Digitek is used to treat patients with abnormal heart rhythms and heart failure.
Digitalis toxicity can cause dizziness, vomiting, nausea, low blood pressure, bradycardia and cardiac instability. Death is also possible from ingesting excess Digitalis. Several reports of illnesses and injuries have already been received.
If you or someone close to you has been injured by Digitek tablets, you should contact an attorney right away! You may be entitled to compensation for your injuries and we can help.
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