Digitek Recall | Beasley Allen On April 25, 2008, drug manufacturer Actavis Totowa issued a Class I recall for Digitek, which is used to treat heart failure and abnormal heart rhythms. The recall came when it was discovered Digitek tablets had been manufactured at twice the intended thickness, doubling their strength and raising the possibility of triggering a toxic reaction. Side effects from the too-strong tablets include nausea, vomiting, low blood pressure, cardiac instability, bradycardia and even death Digitek-legal.com~Site InfoWhoisTrace RouteRBL Check
