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

FDA recall notice · announced July 21, 2021 · Yamtun7

Class I FDA/FSIS Class I: reasonable probability that use will cause serious adverse health consequences or death.

The product

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

Reason for recall

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.

Notes

Distribution: Unknown; unable to determine due to firm's Ebay account being closed.
Lot/code information: All lots distributed 07/01/2019 through 09/28/2020.
Quantity: 36 capsules
Status: Terminated
Products in this recall event:
- Poseidon Platinum 3500 capsule, 1-count per blister card, Distributed by: Poseidon, Made in the USA, UPC 0 95842 05876 0 (D-0654-2021)

Source: U.S. Food and Drug Administration public recall data. This page reports official records and is not legal, medical, or repair advice.