ForeverMen Natural Energy Boost Capsules — Class I drug recall D-0470-2024
Terminated recall by FA Online Inc, reported 2024-05-01, distributed nationwide. Marketed Without an Approved NDA/ANDA: Product was found to contain undeclared sildenafil, an ingredient found
| Recall number | D-0470-2024 |
|---|---|
| Product type | Drug |
| Classification | Class I |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | FA Online Inc, Fresh Meadows, NY, United States |
| Recall initiated | 2024-02-12 |
| Classified | 2024-04-23 |
| Reported by FDA | 2024-05-01 |
| Terminated | 2024-06-13 |
| Distributed | Nationwide (US) |
| Quantity | 400 capsules |
| Reason classes | undeclared allergen, unapproved product |
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.
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/D-0470-2024. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.