← FDA ENFORCEMENT
D-0470-2024Class I

FA Online Inc

Recalling firm
FA Online Inc
Product type
Drug
Status
Terminated
Report date
2024-05-01
Distribution
USA Nationwide. The product was sold via Amazon Market Place.
Firm state
NY
Product quantity
400 capsules
Initiated by
Voluntary: Firm initiated
SPEQ quality domain
Documentation & Change Control
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.

Product description

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

Code / lot info

All lots within expiry

Other recalls SPEQ maps to Documentation & Change Control
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Data: U.S. FDA openFDA enforcement API. Recall details are as reported by the FDA. The quality-domain mapping and severity are a SPEQ editorial interpretation of the recall reason, not an official FDA classification.