FDAFDA · Food and drugs·Recall number D-0654-2021
Poseidon Platinum 3500 capsule, 1-count per blister card, Distributed by: Poseidon, Made in the USA, UPC 0 95842 05876 0
Published July 21, 2021 · Recall initiated: May 11, 2021
Status when published: Terminated — openFDA updates weekly, so this field may not reflect the current status. Always confirm with the official notice.
What's 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
Voluntary: Firm initiated · Press Release
Recall details
- Manufacturer
- Yamtun7
- Distributor
- Unknown; unable to determine due to firm's Ebay account being closed.
- Lot
- All lots distributed 07/01/2019 through 09/28/2020.
- Risk classification
- Class I
- Area (FDA)
- drug
- Country
- United States
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