(Update: Looking for the Catfood Recall or Dogfood Recall List? Click the link.)Lab analysis of V.MAX product samples by the Food and Drug Administration revealed the male enhancement supplement to contain Aminotadalafil, an analogue of Tadalafil.The FDA approves Tadalafil to treat erectile dysfunction (ED), but only with a doctor's prescription.
By unknowingly taking Aminotadalafil, those who use VMAX are being put at risk for
dangerously low blood pressure.
Consumers who have V.MAX in their possession are urged to stop using it immediately and contact their doctor.
March 16, 2007 - Press Release - Cosmos Trading, Inc.Rhino Max (Rhino V Max) supplement productCosmos Trading, Inc. and FDA notified consumers and healthcare professionals of a voluntary nationwide recall of a supplement product sold under the name Rhino Max (Rhino V Max) in 5-tablet boxes or 15-tablet boxes. Lab analysis by FDA of product samples found the product contains Aminotadalafil, an analogue of Tadalafil, an FDA-approved drug used to treat Erectile Dysfunction (ED). FDA advised that this poses a threat to consumers because Aminotadalafil may 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 nitrates. Consumers who have Rhino Max (Rhino V Max) in their possession should stop using it immediately and contact their physician if they experienced any problem that may be related to taking this product.
Labels: bone recall, drug, fda, male enhancement, pharmaceutical, recalls, tadalafil, v-max, v.max, vmax
