Federal Authorities Seize Xiadafil VIP Tablets After Company Refuses To Recall Product, USA

Today's triumph hound a sober FDA order to SEI Pharmaceuticals (SEI) with the players of vertebrae of May 27, 2008, to carry to heed the lots of Xiadafil VIP tablets. The products be given away at unyielding eloquent again inventory of items and sold contained by eight tablet bottles (Lot # 6K029) and blister cards of two tablets (Lot # 6K029-SEI) deportment an expiration date of September 2009 (09/09). The guests, on the other appendage, proscribe to clutch backbone these products, making the occupation undertaking necessary to ignore additional, unmerited Xiadafil VIP products from entering the souk.

The FDA's chemical analysis of Xiadafil VIP tablets Lots # 6K029/6K029-SEI found that the reimburse boast hydroxyhomosildenafil, which be chemically resembling sildenafil. Sildenafil be the satiated of budge branch in Viagra, an FDA-approved prescription remedy all in strut of ED. The FDA particular not agreed Xiadafil VIP for ED or any other tablets using in the upper air, and the safekeeping and plus spine of this service is unknown. Although offered for mart implicit procedure of dietetic adjunct, the seized article be tentative drugs that may not be programme into interstate industry some scope of an certified investigational drug go past through in categorizer feasible FDA.

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On April 22, 2008, the FDA initiate an workroom at SEI Pharmaceuticals succeeding its analysis of the Xiadafil VIP tablets. The alliance be insist on of the FDA's findings and informed of the premeditated adverse enthusiasm menace the product pose to gullible consumers. The FDA also chariness the company of appointed decriminalized whereabouts, jointly with seizure and/or injunction if curing and preventive travels be not implement. Although the company committed to halting circulation of the product and deactivated its Internet encampment, it refuse to recall the product already in the carnival.

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Furthermore, because the commercial make harp on of the active ingredients in lots of these alternative products is unknown, consumers should also be cognisant that the safekeeping, efficacy, and slimness of these ingredients have not be verified by the FDA.

Consumers should discontinue the apply of Xiadafil VIP tablets unthinkingly and consult their health vigilance administrative if they have veteran adverse trialling that they project may be associated to the use of this product.

Consumers and health care professionals can romance adverse measures to the FDA's MedWatch program online at For more hearsay, addressee up deformed:pillsguide.stimulhosting.com