Rhino 7 recall
via email at at any time or by phone at 46 on Monday through Friday between the hours of 9 a.m. Consumers who purchased the product in October, 2019 should stop consuming it and return any unused product to Motto International Corp., Consumers should contact their physician or healthcare provider if they have experienced any problems that may be related to taking or using this drug product.Ĭonsumers with questions regarding this recall can contact Motto International Corp.
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is notifying its customers by email and is arranging for replacement of recalled products, at the request of the customer. Product was sold locally to 2 Dallas convenience stores. The product can be identified by the product labels attached below. The Bull Platinum 30000, Stallion Platinum 30000, Rhino 7 Platinum 30000, and Panther Platinum 30000 products are marketed as dietary supplements for male sexual enhancement and are packaged in 2, 4, and 10 capsule blister pack cards. has not received any reports of adverse events related to this recall. Consumers with diabetes, high blood pressure, high cholesterol, or heart disease often take nitrates and may be the population most likely to be affected. The combination of tadalafil and nitrates may lower blood pressure to dangerous levels which can be life threatening. The presence of tadalafil in these products renders them unapproved drugs for which safety and efficacy has not been established and, therefore, subject to recall.Ĭonsumption of a product with undeclared tadalafil may pose a risk to consumers who take prescription medications containing nitrates (such as nitroglycerin).
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Tadalafil is an FDA approved drug indicated for the treatment of male sexual enhancement. FDA analysis has found Bull Platinum 30000, Stallion Platinum 30000, Rhino 7 Platinum 30000, and Panther Platinum 30000 to be tainted with undeclared tadalafil. is voluntarily recalling all lots of Bull Platinum 30000, Stallion Platinum 30000, Rhino 7 Platinum 30000, and Panther Platinum 30000, to the consumer level. FDA does not endorse either the product or the company.
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When a company announces a recall, market withdrawal, or safety alert, the FDA posts the company’s announcement as a public service.