Digitek® Recall Resources

S&C Related Contents
FDA Digitek (digoxin) Recall Notice
Digitek® Quick Facts
Brand
Digitek®
Status
Recalled
Manufacturer
Actavis Totowa LLC
Side Effects
Digitalis Toxicity
Nausea
Vomiting
Dizziness
Low Blood Pressure
Cardiac Instability
Bradycardia
BREAKING NEWS: On April 25, 2008, the manufacturer of Digitek® (digoxin tablets) issued an urgent nationwide recall of the product due to the possibility that tablets with double the appropriate thickness may have been commercially released. These tablets may contain (2) twice the approved level of active ingredient than it appropriate. The doubling of Digoxin can lead to Digitalis toxicity and other serious life-threatening side effects.
If you or a loved one have taken Digitek or Digoxin tablets and suffered any side effects including Digitalis toxicity, you should contact us immediately. You may be entitled to compensation and we can help.
Digitalis toxicity is a side effect associated with the ingestion of Digitek® (digoxin tablets). Digitalis toxicity can occur from a single exposure or chronic overmedication.
Risks include taking digitalis medications such as digoxin or digitoxin, along with medications that interact with digitalis such as quinidine, verapamil, amiodarone, and others.
Additional symptoms that may be associated with Digitalis toxicity include:
The Defective Drug & Products Liability Litigation Groups at our law firm are an experienced team of trial lawyers that focus exclusively on the representation of plaintiffs in defective drug lawsuits. We are pursuing individual litigation nationwide and currently accepting new Digitek (digoxin tablet) recall and Digitalis toxicity cases in all 50 states.
Attention Attorneys: We do not publish prior verdict/settlements. If you are an attorney and would like to refer us a case or for us to send you a profile of prior award judgments or average referral fees, please visit the attorney referral section of our website.
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