Class III โ€” Low Risk

Low risk โ€” use of or exposure to this product is not likely to cause adverse health consequences.

Extra Strength Headache Relief (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...

Date: August 3, 2020
Company: Ultra Seal Corporation
Status: Terminated
Source: FDA (Drug)

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

Extra Strength Headache Relief (Acetaminophen 250 mg/aspirin 250 mg/Caffeine 65 mg) tablets, 2-tablet packets, Manufactured for: Convenience Valet Glendale Heights, IL 60139,

Quantity: 701,735 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

Affected (2 states)Not affected

About Ultra Seal Corporation

Ultra Seal Corporation has 66 total recalls tracked by RecallDetector.

Related Recalls

Data sourced from the FDA (Drug). Last updated March 26, 2026. View original report