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On May 23, 2003, in cooperation with the FDA, Best Life International, the distributor of Viga and Viga for Women, issued a Viga recall. The Viga recalls advised Viga consumers to immediately discontinue its use. Although Viga is considered a dietary supplement, which is not federally regulated, the Viga recall occurred because of it illegally contained a prescription ingredient that was not on Viga labeling.
Since Viga is sold over the counter and on the Internet, the Viga recall was issued after FDA investigators found the tablets contained the unlabeled prescription drug ingredient sildenafil. Sildenafil can have very serious and deadly effects if interacting with prescription nitrates, an absolute contraindication for sildenafil users that made an immediate Viga recall necessary. The Viga recall should be taken into immediate consideration because of the life threatening lowering of blood pressure that is at risk.
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