Yamtun7 recalls Poseidon Platinum 3500 capsule, 1-count per blister card, Distributed by: Poseidon, Made in the USA, UPC 0 95842 05876 0
Recalled July 21, 2021 · FDA recall D-0654-2021 · Yamtun7
Hazard
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. · FDA Class I
Units
36 capsules
Sold at
Unknown; unable to determine due to firm's Ebay account being closed.
Description
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.
Product
Poseidon Platinum 3500 capsule, 1-count per blister card, Distributed by: Poseidon, Made in the USA, UPC 0 95842 05876 0
Manufacturer(s)
Yamtun7
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →