On April 25, 2008, a nationwide Digitek Tablet Recall was issued for all lots of the heart medication. Manufacturing problems caused some tablets to contain twice as much of the active ingredient as is appropriate. This could result in digitalis toxicity in patients with impaired kidney function, which is a serious and potentially fatal illness. Continued
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Following Digitek Recall, Class Action Suits have been filed
At least two class action suits have been filed on behalf of individuals who used the heart drug Digitek (digoxin). The suits come less than three weeks after all lots of Digitek were recalled on April 25th when it was discovered that some tablets sold over the past year could be twice as thick as is appropriate and contain double the approved amount of active ingredient. Continued
