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Yamtun7 Recalls
1 recall on record · July 21, 2021 to July 21, 2021 · Drugs
July 21, 2021
Drugs
FDA
Yamtun7 recalls Poseidon Platinum 3500 capsule, 1-count per blister card, Distributed by: Poseidon, Made in the USA, UPC 0 95842 05876 0
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.
Yamtun7 Recalls | RecallWatchUSA