Digitek Recall Help: Latest News Regarding the Digitek Recall



Digitek Side Effects Digoxin Toxicity Signs of an Overdose	Digitek Recall Why Was Digitek Recalled?	Digitek Lawsuits A Digitek Attorney Can Help	Digitek News Press Releases




Digitek Recall News Actavis temporarily closes Digitek recall plant over manufacturing problems Drugmaker Actavis has reached an agreement with U.S. health authorities to temporarily close three New Jersey plants in order to resolve violations of Food and Drug Admininstration “Good Manufacturing Practices” that occurred there. The company agreed to close two manufacturing plants and a third packaging plant until it could show that it was in compliance with the FDA regulations. Kentucky man files Digitek lawsuit following wife’s death A Kentucky man has filed a Digitek lawsuit against the distributor of the heart medication on behalf of his deceased wife. John Conte alleges that his wife, Scottye, died in October 2007 after suffering digoxin toxicity from an excess dose of Digitek. Congress seeking information about the Digitek recall Congress has sent a letter to officials with the Food and Drug Administration asking the agency to provide it with more information about a series of drug recalls by Actavis Totowa, including one that involved Digitek. Actavis issued a Digitek recall in April 2008 after learning that some tablets of the heart medication were manufactured at twice the normal dose. Nine federal Digitek lawsuits filed in N.J. Nine federal Digitek lawsuits have been filed by patients in New Jersey against the drug’s manufacturer, Actavis Totowa. These lawsuits allege that Digitek was a dangerous and defective product because of improper manufacturing practices, putting patients at an increased risk of serious injury due to digoxin toxicity. At least one patient involved in the Digitek lawsuits died as a result of side effects they suffered after taking the drug. Actavis received two warnings because of “adulterated” drugs In the wake of the Digitek recall, reports have emerged that Actavis Totowa, the manufacturer of the heart drug, received two warning letters from the Food and Drug Administration in 2006 and 2007. The letters charged the company with failing to properly report adverse events for drugs including Digitek and for failing to follow “Good Manufacturing Practices” to ensure the safety of its products. « More Digitek Recall News »

Contact us for free information about your Digitek/Digoxin Case

* Name:

* Email (email or phone required) :

* Phone # (email or phone required):

Please tell us about your case:

How long did you take Digitek:

Have you tested positive for Digoxin toxicity?
Yes No

Have you or a loved one suffered from any of the following?

Heart Attack	Death
Stroke	None

I am currently represented by an attorney.

I would like to receive emails from Hissey Kientz about Digitek and other drugs and devices.

Hissey Kientz LLP - Digitek Lawsuit attorneys

Digitek Recall Help Firm
Contact Hissey Kientz, LLP - Austin, TX

The Hissey Kientz, LLP attorneys represent victims from Alabama, Alaska, Arizona, Arkansas, California, Colorado, Connecticut, D.C., Delaware, Florida, Georgia, Hawaii, Idaho, Illinois, Indiana, Iowa, Kansas, Kentucky, Louisiana, Maine, Maryland, Massachusetts, Michigan, Minnesota, Mississippi, Missouri, Montana, Nebraska, Nevada, New Hampshire, New Jersey, New Mexico, New York, North Carolina, North Dakota, Ohio, Oklahoma, Oregon, Pennsylvania, Rhode Island, South Carolina, South Dakota, Tennessee, Texas, Utah, Vermont, Virginia, Washington, West Virginia, Wisconsin and Wyoming.

Address: 9442 North Capital of Texas Hwy Suite 400 Austin TX 78759 Phone: (512) 320-9100
Administration

Digitek Recall News