Delray Beach, FL, United States
Yamtun7 recalls
1 recall recorded since 2018, most recently on 11 May 2021. None are listed as ongoing. Status and classification are as published by the FDA.
Recalls1
Ongoing (FDA)0
Terminated or completed1
Class I (FDA)1
Terminated Class I Drugs
- Recall started
- 11 May 2021
- Terminated
- 12 July 2023
- Reason
- 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.
- Distribution
- Unknown; unable to determine due to firm's Ebay account being closed.
- Initiated
- Voluntary: Firm initiated
- 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
A terminated FDA recall means the FDA has determined that all reasonable efforts to remove or correct the product have been made. What statuses mean.