Jump to Main Content

Bertek, UDL, and Digitek May Contain Twice the Approved Active Ingredient

Digitek, a drug used to treat heart failure and abnormal heart rhythms, has been recalled because some tablets contain twice the approved level of active ingredient. These tablets can cause serious injuries--including low blood pressure, cardiac instability, and death. Please contact us if you or a loved one has suffered injury following ingestion of Digitek. You can reach us at 1-800-464-2266.

The drug is distributed by Mylan Pharmaceuticals and sold under the labels "Bertek" or "UDL".

Download the FDA Recall Notice (PDF)