CLASS I Drug recall · Reported 1 May 2024 · FDA Enforcement Report
ForeverMen Natural Energy Boost Capsules recalled by FA Online
FA Online is recalling ForeverMen Natural Energy Boost Capsules, distributed nationwide in the US. The recall was initiated on 12 Feb 2024 and the FDA has classified it as Class I.
Check your package
Check the lot number on your package against the affected lots. If it matches, contact the pharmacy that dispensed it or your prescriber before stopping any medication.
Recall details
- Recall number
- D-0470-2024
- FDA event ID
- 94339
- Recalling firm
- FA Online, Fresh Meadows, NY
- Classification
- Class I
- Status
- Terminated
- Recall initiated
- 12 Feb 2024
- FDA classified
- 23 Apr 2024
- Reported
- 1 May 2024
- Type
- Voluntary: Firm initiated
- Customers notified by
- Press Release
- Reason category
- Labeling Errors
Timeline
| 12 Feb 2024 | Recall initiated by company | |
| 23 Apr 2024 | Classified by FDA | +71 days |
| 1 May 2024 | Published in enforcement report | +8 days |
Companies usually start a recall weeks before the FDA classifies and publishes it; the gap above is that lag.
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 as listed by the FDA
ForeverMen Natural Energy Boost Capsules, packaged in a box containing a 10-count blister card.
Where it was distributed
USA Nationwide. The product was sold via Amazon Market Place.
Stores named: Amazon, Online Retailers
Questions about this recall
Is ForeverMen Natural Energy Boost Capsules recalled?
Yes. FA Online recalled ForeverMen Natural Energy Boost Capsules on 12 Feb 2024. The recall is Class I and its status is Terminated. Recall number D-0470-2024.
Why was it recalled?
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.
Which lots are affected?
All lots within expiry
Where was it sold?
USA Nationwide. The product was sold via Amazon Market Place.
What should I do if I have it?
Check the lot number on your package against the affected lots. If it matches, contact the pharmacy that dispensed it or your prescriber before stopping any medication.
What does Class I mean?
Class I is the most serious FDA recall category: there is a reasonable probability that using the product will cause serious health consequences or death.
Read the official FDA notice · Source record retrieved 21 Sep 2026. The FDA describes openFDA data as unvalidated; the official notice takes precedence. This page reports the record and gives no medical advice.