Key Takeaway
ForeverMen Natural Energy Boost Capsules, packaged in a box containing a 10-count blister card. by FA Online Inc was recalled on February 12, 2024. The hazard: Marketed Without an Approved NDA/ANDA: Product was found to contain undeclared sildenafil, an ingredient found in FDA approved products for the treatm...
ForeverMen Natural Energy Boost Capsules, packaged in a box containing a 10-count blister card.
Description
ForeverMen Natural Energy Boost Capsules, packaged in a box containing a 10-count blister card.
Hazard / 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.
Class I: Dangerous or defective product that could cause serious health problems or death.
Class I is the most serious recall classification used by the FDA, indicating a reasonable probability of serious health consequences or death.
Products Affected
ForeverMen Natural Energy Boost Capsules, packaged in a box containing a 10-count blister card.
DrugsCompany Information
FA Online Inc
Fresh Meadows, NY, United States
View all 1 recalls by FA Online Inc →Distribution
USA Nationwide. The product was sold via Amazon Market Place.
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Frequently Asked Questions
Is this recall still active?
Check the status badge at the top of this page. "Ongoing" means the recall is still active and you should follow the remedy instructions. "Completed" or "Terminated" means the recall process has concluded, though the safety issue remains relevant for any unrepaired products.
How do I check if my product is affected?
Compare the model number, lot code, serial number, or date range listed in the recall notice with the information on your product's label or packaging. For vehicles, check your VIN at NHTSA.gov/Recalls.
What remedy is available for this recall?
Check the remedy section above or contact the manufacturer directly for current remedy options.
Where can I find the original recall notice?
This recall was issued by FDA Drug. Visit the agency's official website for the original notice.