Morristown, NJ - The manufacturer of Digitek digoxin tablets is recalling the product, saying that it may have accidentally released pills that are double the normal thickness, carrying twice the ...

All lots of Digitek tablets, used to treat heart failure and abnormal heart rhythms, are being recalled because some were accidentally made double-strength. The recall was issued because some of those ...

Actavis has issued a nationwide recall of Digitek (digoxin tablets) due to the possibility that tablets with double-thickness, containing twice the approved level of active ingredient, may have been ...

WASHINGTON, April 28 (UPI) -- The U.S. Food and Drug Administration announced the recall of Digitek-brand digoxin heart tablets because of a potential safety risk. The FDA said Actavis Totowa LLC, ...

Digitek has an excess-API history. Actavis initiated a Class 1 recall of the drug in the spring of 2008 for pills that potentially contained twice the approved level of API digoxin, the story said.

Digitek accounted for roughly one-half of all the digoxin on the market in the United States. Barbara Guthrie of Denver, Colorado, whose husband, James Guthrie died on August 18, 2007, after taking ...

WASHINGTON (Reuters) - Generic drugmaker Lannett Co on Thursday said it is working with U.S. regulators to ensure a safe supply of the heart failure drug digoxin, following a recall of another version ...