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Urgent Recall: Digitek Double Dose Tablets may Cause Overdose |
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September 7, 2008. By Jane Mundy.
 Lodi, CA: "It blows my mind that the FDA knew about Actavis Totowa, the maker of Digitek and its quality control problems back in 2006," says Carol M. "Why wasn't it shut down two years ago? I understand that the FDA is very lenient with pharmaceutical companies and gives them several chances to clean up their act, but this has gone too far." |
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September 7, 2008. By Heidi Turner.
 Phoenix, AZ: Isaac S. had a hernia repair 2003, during which Kugel Mesh was used. Since that time, he has had two more surgeries to repair problems caused by the mesh. He says he does not want anyone else to go through what he has been through. |
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Emerging Legal Issues
[Free Instant Email Alerts]- Sprouters Northwest Recalls Alfalfa Sprout Products for Possible Salmonellosis (Sep-5-08)
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Settlements and Verdicts - Cases Won Every Day
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