Yamtun7 Recalls Poseidon Platinum 3500 Due to the Presence of Undeclared Tadalafil and Sildenafil

Yamtun7 recalled all lots of Poseidon Platinum 3500 to the consumer level due to potential health risk.

The Food and Drug Administration (FDA)  has found the product to contain undeclared tadalafil and sildenafil. 

Tadalafil and sildenafil are drugs known as phosphodiesterase (PDE-5) inhibitors that are found in FDA approved products for the treatment of male erectile dysfunction.

The presence of tadalafil and sildenafil in Poseidon Platinum 3500 makes it an unapproved new drug, therefore subject to recall.

Consumers with underlying medical issues who take Poseidon Platinum 3500 with undeclared tadalafil and sildenafil may experience serious health risks.

The recalled product has been distributed nationwide.

Yamtun7 has notified its customers by this press announcement and via e-mail of this recall. The company advises consumers that have Poseidon Platinum 3500 should stop using it and immediately destroy them.

Yamtun7 urges consumers to contact their physicians or healthcare provider if they have experienced any problems that may be related to taking or using this drug product.

There have been no reports of adverse events related to this recall thus far.


© Fourth Estate® — All Rights Reserved.
This material may not be published, broadcast, rewritten or redistributed.