# FDA recall D-0470-2024

> **FA Online Inc** · Class I · drug recall initiated 2024-02-12.

## Product

ForeverMen Natural Energy Boost Capsules, packaged in a box containing a 10-count blister card.

## Reason for recall

Marketed Without an Approved NDA/ANDA: Product was found to contain undeclared sildenafil, an ingredient found in FDA approved products for the treatment of male sexual enhancement, making this unapproved drug.

## Distribution

USA Nationwide. The product was sold via Amazon Market Place.

## Key facts

- **Recall number:** D-0470-2024
- **Recalling firm:** FA Online Inc
- **Classification:** Class I
- **Product type:** drug
- **Status:** Terminated
- **Initiation date:** 2024-02-12
- **Report date:** 2024-05-01
- **Termination date:** 2024-06-13

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Fresh Meadows, NY, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=D-0470-2024

## Citation

> AI Analytics. FDA recall D-0470-2024. Retrieved 2026-07-26 from https://api.ai-analytics.org/recall/D-0470-2024. Source: US FDA. Licensed CC0.

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*[Dataset catalog](/datasets/) · [FDA recalls dataset](/datasets/fda-recalls) · CC0 1.0*
