FDA Alerts
FDA Recalls RegenArouse
Regeneca , Inc. notifed the public of a nationwide recall of RegenArouse , Lot Number 130100. FDA lab analysis confirmed the presence of Tadalafil , an FDA-approved drug used as treatment for male Erectile Dysfunction (ED), making this product an unapproved new drug.
Not for the Faint of Heart
Kanec USA Inc. is voluntarily recalling all lots of its male enhancement capsules due to unapproved use of an erectile dysfunction drug that could lead to potentially dangerous drug interactions.