Low risk — use of or exposure to this product is not likely to cause adverse health consequences.
Pain Relief Maximum Strength (Acetaminophen 250 mg/aspirin 250 mg/Caffeine 65 Recalled by Ultra Seal Corporation Due to Failed Stability Specifications: Out-of-Specification (OOS) results for the...
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
Pain Relief Maximum Strength (Acetaminophen 250 mg/aspirin 250 mg/Caffeine 65 mg) tablets, 2-tablets per packet, Manufactured for Select Corporation, Carrollton, TX 75007
Quantity: 4,666,355 packets
Why Was This Recalled?
Failed Stability Specifications: Out-of-Specification (OOS) results for the Aspirin related compound Salicylic Acid was observed.
Where Was This Sold?
This product was distributed to 2 states: IL, TX
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