Erectile Dysfunction Supplement
On July 28, 2008 the U.S. Food & Drug Administration in association with Jack Distribution, LLC and its wholesale distributors G & N works, Inc. and Devine Distribution, Inc. issued a nationwide recall of Rize 2 The Occasion Capsules and Rose 4 Her Capsules.
These products are marketed as dietary supplements. In routine lab testing the FDA found the product contains potentially harmful, undeclared ingredients. FDA asserts that its chemical analysis revealed that Rize 2 The Occasion and Rose 4 Her contain thiomethisosildenafil, an analog of sildenafil, the active ingredient of a FDA-approved drug used for Erectile Dysfunction (ED).
This undeclared chemical poses a potential threat to consumers because it may interact with nitrates found in some prescription drugs (such as nitroglycerin) and may lower blood pressure to dangerous levels.
Do I Have a Lawsuit?
If you or somebody you know has suffered a serious adverse event related to the Rize 2 The Occasion and Rose 4 Her recall, you should contact us immediately. You may be entitled to compensation for your injuries and we can help.
On July 24, 2008 the U.S. Food and Drug Administration & U.S. Marshals seized nearly $74,000 worth of Xiadafil VIP tablets, Lots 6K029 and 6K209-SEI, distributed by SEI Pharmaceuticals, Inc. of Miami, Florida.
The recall and seizure were initiated after the company refused to issue a recall of their products after a formal written request to do so by the FDA.
Although marketed as a dietary supplement to treat erectile dysfunction (ED) and for sexual enhancement, these lots represent an illegally marketed drug containing an undeclared ingredient.
ED is a common problem in men who have diabetes, high blood pressure, high cholesterol, or heart disease. Because they may have been advised against taking ED drugs, men with these conditions may seek alternative products like Xiadafil VIP tablets because they are marketed as “all natural” or as not containing the active ingredients in approved, prescribed ED drugs. Furthermore, because the manufacturing source of the active ingredients in many of these alternative products is unknown, consumers should also be aware that the safety, efficacy, and purity of these ingredients have not been verified by the FDA.
Do I Have a Lawsuit?
If you or somebody you know has suffered from a serious side effect related to Xiadafil VIP tablets, you should contact us immediately. You may be entitled to compensation for your injuries and we can help.
On July 23, 2008 EG Labs, LLC in association with the U.S. Food & Drug Administration issued an urgent nationwide recall of Viapro.
According to the FDA, “EG Labs, LLC. is conducting this recall after being informed by representatives of the Food and Drug Administration (FDA) that lab analysis by FDA of a sample from one lot of the product revealed that it contained a potentially harmful undeclared ingredient, thio-methisosildenafil. FDA asserts that this ingredient is an analog of sildenafil. Sildenafil is the active chemical ingredient of an FDA-approved drug used for Erectile Dysfunction (ED) in men to enhance sexual performance.”
The use of undeclared chemicals pose a threat to consumers because they may harmfully interact with nitrates found in some prescription drugs (such as nitroglycerin) and may lower blood pressure to dangerous levels. Consumers with diabetes, high blood pressure, high cholesterol, or heart disease often take such nitrates.
If you or somebody you know has suffered from a serious injury related to Viapro, you should contact us immediately. You may be entitled to compensation for your injuries and/or loss.
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