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Please fill out the form below to see if you have a Digoxin recall case.
First Name:
Last Name:
Phone: -
Alt. Phone: -
Date Started Digitek:
Date Stopped Digitek:
Oral Dosage: .125mg .25mg
How many times per day was Digitek taken?
Date of last prescription refill for Digitek before injury:
What injuries do you allege from Digitek?
When did the injury occur?
If death from Digitek is alleged, was an autopsy performed? Yes No
If Yes, by whom?
If No, was any bloodwork taken? Yes No
Where was bloodwork taken?
When was bloodwork taken?
Please note any significant past medical history:
duragesic Diabetes Medication Increases Risk of duragesic Heart Failure

Do you have a Digitek lawsuit?
Looking for Personal Injury and Wrongful Death Lawyers?

On April 25, 2008 Actavis Totowa LLC initiated a recall of Digitek® (digoxin tablets, USP, all strengths) for oral use.


The products are distributed by Mylan Pharmaceuticals Inc., under a "Bertek" label and by UDL Laboratories, Inc. under a "UDL" label.

The voluntary all lot recall is due to the possibility that tablets with double the appropriate thickness may have been commercially released. These tablets may contain twice the approved level of active ingredient than it appropriate.

If you or a loved one has been harmed because of the Digiteck recall then you need a competent personal injury/wrongful death law firm by your side.

Please contact Monheit Law for a free consultation to find out what your legal options are.








Recalls Digitek Heart Drug

Law Offices of Michael Monheit 1368 Barrowdale Road  Rydal, PA  19046
Call Us Toll Free: 866-761-1385 P: 215-840-6573 E: Michael@Monheit.com