Yamtun7 Recalls

FDA
1
Total Recalls
1
Agencies
Jul 2021
First Recall
Jul 2021
Latest Recall

Showing 1-1 of 1 recalls

FDA

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

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.