Poseidon Platinum 3500 capsule recalled over undeclared sildenafil

Recall date

May 11, 2021

Source

U.S. Food & Drug Administration (FDA) — enforcement report

Official notice title

Yamtun7 recalls Poseidon Platinum 3500 capsule, 1-count per blister card, Distributed by: Poseidon, Made in the USA, UPC 0 95842 05876 0

Recall number

D-0654-2021

FDA classification

Class I

Brand / firm

Yamtun7

Sold / distributed

Unknown; unable to determine due to firm's Ebay account being closed.

Why it was recalled

Marketed Without An Approved NDA/ANDA: Product found to contain undeclared sildenafil and tadalafil making them unapproved drugs for which the safety and efficacy have not been established and therefore subject to recall.

Class I is the FDA’s most serious recall level: there is a reasonable probability that using this product will cause serious harm or death.

What was recalled

Poseidon Platinum 3500 capsule, 1-count per blister card, Distributed by: Poseidon, Made in the USA, UPC 0 95842 05876 0