date:May 18, 2018
Shoreside Enterprises, Inc. is voluntarily recalling 7K （Lot specific: Lot #RO） and Poseidon 4500 （Extreme 1000 mg） （Lot specific: Lot #20117BL） to the consumer level. FDA analysis found the samples of these products to contain undeclared Sildenafil and/or Tadalafil. Sildenafil and Tadalafil are active ingredients in two FDA-approved prescription drugs used for the treatment of erectile dysfunction （ED）。 The presence of Sildenafil and Tadalafil renders them unapproved drugs for which