Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
PremierZen Extreme 3000 Recalled by QMart Due to Marketed without Approved NDA/ANDA: FDA analysis results obtained...
What You Should Do
Stop using this product immediately. Do not consume, use, or distribute it.
Return the product to the place of purchase for a full refund. If you have questions, contact QMart directly.
Affected Products
PremierZen Extreme 3000, Male Sexual Performance Enhancement, 1 Capsule, UPC 728175421887
Quantity: 500 boxes
Why Was This Recalled?
Marketed without Approved NDA/ANDA: FDA analysis results obtained the presence of tadalafil and/or sildenafil.
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About QMart
QMart has 4 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Drug). Last updated March 26, 2026. View original report