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Over the past decade, Actavis (officially known as Actavis Totowa LLC) has become one of the top five producers of generic medications worldwide. Manufacturing over 650 different medicines, Actavis generates over $2 billion in revenues each year.
Among the various types of medication produced by Actavis are:
Currently, Actavis has operations in 40 countries. While the company's international headquarters are located in Iceland, its U.S. operations are based in New Jersey.
Since Actavis was started in 1956, this pharmaceutical manufacturer's products have provided relief for millions of people worldwide.
However, many have also been injured after taking (or using) Actavis medication, as some of these drugs have been found to cause serious side effects. To date, over 60 Actavis products have been recalled by the Food and Drug Administration (FDA).
Actavis product recalls have been issued for:
For more Actavis products, view a complete list of recalled Actavis products.
Severe injuries sustained after taking Actavis products that have been recalled range from arrhythmia and stroke to severe allergic reaction and wrongful death.
Although a number of Actavis products have been recalled, it's likely that:
Patients who have been injured after taking Actavis products (and families of patients who have died after taking Actavis products) will:
Prospective plaintiffs can learn more about their legal rights and find out if they have a defective drug claim by meeting with an experienced personal injury attorney for a free initial consultation.
Have you or a loved one been seriously injured after taking a medication produced by Actavis? If so, contact us today to consult with an experienced defective drug attorney who will thoroughly evaluate your case and help you pursue legal recourse.
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