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Hissey Kientz Concerned That Patients Have Not Been Provided With Crucial Information About Digitek Recall Despite the Dangers of Digoxin Toxicity
Date:8/16/2008

otices were issued after an FDA inspection earlier this year revealed that the company had continued to violate “standards for good manufacturing practices,” according to a statement by the company, even after it had received two previous warning letters for similar infractions.

Digitek tablets manufactured by Actavis Totowa were distributed by UDL Laboratories and Mylan Pharmaceuticals. Tablets distributed by UDL were sold under the label “UDL,” while those distributed by Mylan were sold under the name “Bertek.” Patients who were taking Digitek before the recall notice was issued may wish to speak with their doctors to discuss alternate forms of treatment.

Dozens of patients who suffered severe injuries after using Digitek have filed lawsuits against the manufacturer and distributors of the drug. These lawsuits have alleged that Digitek was dangerously and defectively manufactured, putting patients at risk of severe and potentially fatal side effects due to an overdose.

About Hissey Kientz, LLP
http://www.hkllp.com/ [Hissey Kientz, LLP] is currently accepting cases involving individuals who may have been injured as a result of a Digitek overdose. Hissey Kientz, LLP also represents those who contracted mesothelioma or lung cancer as a result of asbestos exposure, and those injured by the Ortho Evra patch, Trasylol, the Composix Kugel mesh patch, the Duragesic patch (fentanyl), gadolinium MRI contrast dyes or other defective drugs and devices. To learn more about the firm and other drug cases, visit Hissey Kientz, LLP (www.hkllp.com) or call toll-free at (866) 275-4454.

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