# FDA recall D-0654-2021

> **Yamtun7** · Class I · drug recall initiated 2021-05-11.

## Product

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

## 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.

## Distribution

Unknown; unable to determine due to firm's Ebay account being closed.

## Key facts

- **Recall number:** D-0654-2021
- **Recalling firm:** Yamtun7
- **Classification:** Class I
- **Product type:** drug
- **Status:** Terminated
- **Initiation date:** 2021-05-11
- **Report date:** 2021-07-21
- **Termination date:** 2023-07-12

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Delray Beach, FL, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=D-0654-2021

## Citation

> AI Analytics. FDA recall D-0654-2021. Retrieved 2026-06-25 from https://api.ai-analytics.org/recall/D-0654-2021. Source: US FDA. Licensed CC0.

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