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Nationwide Digitek Recall Lawsuit & Claim Information Attorneys

Digitek has recently become the subject of a Class 1 FDA recall for all dosages of Digitek tablets. The defective tablets were manufactured by Actavis Totowa, and have been reported to contain a double dose of the active ingredient. This mistake poses serious medical concerns. Medical providers have found that tablets subject to the Digitek recall, if ingested, can result in severe medical complications, generally caused by digitalis toxicity, which is a medical condition that can lead to very serious side effects, sometimes including death.

The recall of Digitek tablets are sold under the labels "UDL" and "Bertek" and are distributed by Mylan Pharmaceuticals. If you or a loved one has experienced negative side effects after taking Digitek tablets subject to the recall, please call our lawyers for a free, no obligation consultation at (877) 494-9949.

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