Reported Jul 21, 2021 · Terminated
Poseidon Platinum 3500 capsule, 1-count per blister card, Distributed by: Poseidon, Made in the USA, UPC 0 95842 05876 0
Yamtun7
High riskUsing this product could cause serious injury, illness or death — stop using it now.What you should do
Stop using the affected lot and contact the recalling firm for the return or refund process. Check the FDA enforcement report for lot-level detail.
Firm contact: Yamtun7 · 955 Egret Cir · Delray Beach, FL · 33444-7603
Is this the product you have?
Poseidon Platinum 3500 capsule1-count per blister card
- Distributed byPoseidon, Made in the USA, UPC 0 95842 05876 0
- Lot codes and dates
- All lots distributed 07/01/2019 through 09/28/2020.
- Amount recalled
- 36 capsules
Why it was recalled
Stop using this product now
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.
Using this product could cause serious injury, illness or death — stop using it now.
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