Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
PAINAID PMF Premenstrual Formula (acetaminophen 500 mg Recalled by Ultra Seal Corporation Due to cGMP deviations
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 Ultra Seal Corporation directly.
Affected Products
PAINAID PMF Premenstrual Formula (acetaminophen 500 mg, pamabrom 25mg) 2 caplet packets, Dist. by ZEE Medical Distributors, LLC Mason, OH 45040, NDC 42961-0046-03
Quantity: 769,200 packets
Why Was This Recalled?
cGMP deviations
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About Ultra Seal Corporation
Ultra Seal Corporation has 66 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Drug). Last updated March 26, 2026. View original report