Yamtun7: Drug Recall
Recall #D-0654-2021 · 05/11/2021
Class I: Dangerous
Recall Details
- Recall Number
- D-0654-2021
- Classification
- Class I
- Product Type
- Drug
- Recalling Firm
- Yamtun7
- Status
- Terminated
- Date Initiated
- 05/11/2021
- Location
- Delray Beach, FL, United States
- Voluntary/Mandated
- Voluntary: Firm initiated
- Product Quantity
- 36 capsules
Reason for Recall
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.
Product Description
Poseidon Platinum 3500 capsule, 1-count per blister card, Distributed by: Poseidon, Made in the USA, UPC 0 95842 05876 0
Distribution Pattern
Unknown; unable to determine due to firm's Ebay account being closed.
Data from FDA openFDA enforcement reports. This site is not affiliated with or endorsed by the FDA. Recall information may be updated by the FDA at any time.