FDAMay 11, 2021drug
Poseidon Platinum 3500 capsule, 1-count per blister card, Distributed by: Poseidon, Made in the USA, UPC 0 95842 05876 0
Official recall recorded by the U.S. Food & Drug Administration.
The 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.
What to do
FDA enforcement status: Terminated
Brands named
yamtun7
UPCs
095842058760
Recall history
No related federal recalls on record for this brand yet.
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