Digitek Recall By The FDA Announcement 
created by astechno1 on August 2, 2008 9:03 PM
The FDA has recently released a Class 1 Digitek recall for all strengths of Digitek tablets. The tablets, manufactured by Actavis Totowa, may possibly contain a double dose of the active ingredient in Digitek (digoxin).
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Digitek Recall By The FDA Announcement
Recalled Digitek tablets cause severe illness, digitalis toxicity, and may result in death. These side effects are serious, dangerous, and life altering.
by astechno1 on August 2, 2008 9:04 PM