Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
STREE OVERLORD capsules Recalled by A&H Focal Inc. Due to Marked Without An Approved NDA/ANDA: FDA analysis found...
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 A&H Focal Inc. directly.
Affected Products
STREE OVERLORD capsules, 3800 mg, 4-count bottle, labeling is in foreign language
Quantity: unknown
Why Was This Recalled?
Marked Without An Approved NDA/ANDA: FDA analysis found these products to contain sildenafil, an FDA approved drug for the treatment of erectile dysfunction, making these products unapproved drugs for which safety and efficacy have not been establish and therefore, subject to recall.
Where Was This Sold?
This product was distributed to 2 states: NJ, NY
About A&H Focal Inc.
A&H Focal Inc. has 21 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Drug). Last updated March 26, 2026. View original report