Actavis issues recall of digoxin heart medication.

Our lawyers are currently offering a free case review to those who believe they have been harmed by digoxin Digitek tablets.

A Class I recall was issued by Actavis Totowa LLC on April 25, 2008 for all lots of the heart medicine Digitek (generic name digoxin) because some have been found to contain twice the approved levels of active ingredient than is appropriate.

Unfortunately, this digoxin recall comes too late for the families whose loved ones ingested the potentially deadly digoxin dose.

According to the Food and Drug Administration, several reports of illnesses and injuries have been received related to digoxin. This, in turn, sparked the recall.

Concerned family members have already come forward to say the death of a loved one was caused by defective digoxin tablets. If you or a family member were harmed by Digitek (digoxin), please complete the form below for a free review of your potential case. A representative of our firm will be in touch
see also:

Overdosed Digitek Digitek Recalled Due to Possible Overdosed Tablets--Drug Lawyers Info
Some Overdosed Digitek Heart Medicine Sparks Recall--Free lawsuit info

Digoxin Recall Drug Maker Issues Recall of Digoxin (Brand Name Digitek)--Lawyers
Digoxin recall sparks potential lawsuits--Get a free case review

Digitek Lawsuits Our Attorneys Investigate Potential Digitek Lawsuits--Free Case Review
Double-strength Digitek sparks possible lawsuits -lawyers review cases

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