FDA Drug recall D-0470-2024
ForeverMen Natural Energy Boost Capsules, packaged in a box containing a 10-count blister card
- FDA Drug
- Class I
- terminated
- Published 2024-05-01
On 2024-05-01 the FDA classified a Class I recall of ForeverMen Natural Energy Boost Capsules, packaged in a box containing a 10-count blister card by Fa Online, citing 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 enhancemen….
Read the official FDA Drug notice
| Agency | FDA Drug |
|---|---|
| Recall number | D-0470-2024 |
| Classification | Class I |
| Status | terminated |
| Initiated | 2024-02-12 |
| Published | 2024-05-01 |
| Last updated | 2026-09-13 11:52 UTC |
| Company | Fa Online |
| Distribution | US |
Product
ForeverMen Natural Energy Boost Capsules, packaged in a box containing a 10-count blister card.
Reason
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.
Identifiers
| code_info | All lots within expiry |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:52 UTC. Current status: terminated.
Source
Official record: https://api.fda.gov/drug/enforcement.json?search=recall_number:%22D-0470-2024%22
RecallRadar indexes public recall notices from the FDA, USDA FSIS, and CPSC. The official agency notice is the authoritative source. Always confirm details at the linked source before acting.