Serious health hazard — there is a reasonable probability that use of or exposure to this product will cause serious adverse health consequences or death.
X-ROCK For Men Recalled by XRock Industries, LLC Due to Marketed Without an Approved NDA/ANDA: product tested positive...
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 XRock Industries, LLC directly.
Affected Products
X-ROCK For Men, Dietary Supplement, Manufactured by CRM Laboratories, Distributed by XRock Industries, PO Box 120863, Ft. Lauderdale, FL 33312, 0 00309 50792 7. UPC on labeling is: 0 00309 50792 7. UPC in Press Release is: 0030950792.
Quantity: 215,000 capsules
Why Was This Recalled?
Marketed Without an Approved NDA/ANDA: product tested positive for PDE-5 Sildenafil and PDE-5 Hydroxythiohomosildenafil. Hydroxythiohomosildenafil is an analog of sildenafil, an FDA approved prescription drug for Erectile Dysfunction (ED).
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About XRock Industries, LLC
XRock Industries, LLC has 1 total recall tracked by RecallDetector.
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Data sourced from the FDA (Drug). Last updated March 26, 2026. View original report