Weitz & Luxenberg is no longer taking Digitek cases

Weitz & Luxenberg has been contacted by the families of those whose deaths may have be due to defective double-strength 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 recall comes too late for the families whose loved ones ingested Digitek. Some have come forward to say the defective tablets were the cause of their relatives' death.

The Actavis press release on the recall can be found at the FDA website.

If you believe Digitek was responsible for the death of a loved one, please complete the form below for a free evaluation of your potential lawsuit.

A representative of our firm will be in touch shortly.

see also:

Digitek & Deaths Digitek Recall: Families Cite Defective Tablets as Cause of Deaths
Deaths cited as due to double-strength Digitek--Free lawsuit review

Digitek Death Lawyers: Digitek Drug Recall--Incidences of Death and Serious Injury
Deaths reported may be due to defective Digitek--Free Lawsuit Info

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