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Digitek manufacturing defect results in recall

On April 25, 2008 Actavis Totowa LLC, the U.S. a division of the pharmaceutical company Actavis Group issued a nationwide recall on the drug digitek. The recall was initiated as a result of a manufacturing defect whereby pills that are approximately double the normal size may have been released for consumer purchase.

Digitek is distributed in the United States by UDL Laboratories, Inc. under a "UDL" label. and by Mylan Pharmaceuticals, Inc. under a "Bertek" label.

The larger than normal pills pose the risk of severe injury for those who take them resulting in many potential side effects and potentially death.

If you or someone you know may have suffered personal injury of death as a result of taking Digitek contact Grossman Law Offices immediately for a free consultation.

Posted by: Dallas personal injury attorney E. Michael Grossman | Posted on: 9/8/2008 | Comments (0)

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