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 shortly.
see also:
Overdosed Digitek
Digitek Recalled Due to Possible Overdosed Tablets--Drug Lawyers InfoSome Overdosed Digitek Heart Medicine Sparks Recall--Free lawsuit info
Digoxin Recall
Drug Maker Issues Recall of Digoxin (Brand Name Digitek)--LawyersDigoxin recall sparks potential lawsuits--Get a free case review
Digitek Lawsuits
Our Attorneys Investigate Potential Digitek Lawsuits--Free Case ReviewDouble-strength Digitek sparks possible lawsuits--lawyers review cases
