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Earlier this week, the Food and Drug Administration (FDA) requested that a drug company based out of Florida recall their dietary supplement.

The drug recalled is known as Xiadafil VIP Tabs and is manufactured by SEI Pharmaceuticals.

Drug Found to be Harmful

According to the FDA, the medication, which is typically sold in eight tablet bottles or blister cards of two tablets, was found to be potentially harmful to patients.

Xiadafil was found to pose threats to a patient’s blood pressure and can also cause other life-threatening illnesses.

The lots that are being recalled reportedly have an expiration date of September 2009.

FDA Warns Consumers About Dietary Supplement

The FDA is now advising consumers not to purchase the dietary supplement and claim that they are prepared to take further legal action if the tablets are not immediately pulled from shelves.

Even though Xiadafil is reportedly sold as being “all natural” the tabs supposedly contain illegal ingredients that carry many risks.

“Because these products are labeled as ‘all natural dietary supplements,’ consumers may assume that they are harmless and pose no health risk” explains Janet Woodcock, director of the FDA’s Center for Drug Evaluation and Research. “But this just isn’t the case.”

(Source: FDA News)

Have you been harmed by a drug that has been recalled? If so, please contact us to speak with an experienced and trustworthy attorney who will enable you to receive the legal advice you need and deserve.