PlainRecalls
FDA Drug Low Class III Terminated

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,

Reported: August 26, 2020 Initiated: August 3, 2020 #D-1513-2020

Product Description

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,

Reason for Recall

Failed Stability Specifications: Out-of-Specification (OOS) results for the Aspirin related compound Salicylic Acid was observed.

Details

Recalling Firm
Ultra Seal Corporation
Units Affected
701,735 packets
Distribution
Product was shipped to two distributors in IL and TX who may have further repackaged and distributed the product.
Location
New Paltz, NY

Frequently Asked Questions

What product was recalled?
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,. Recalled by Ultra Seal Corporation. Units affected: 701,735 packets.
Why was this product recalled?
Failed Stability Specifications: Out-of-Specification (OOS) results for the Aspirin related compound Salicylic Acid was observed.
Which agency issued this recall?
This recall was issued by the FDA Drug on August 26, 2020. Severity: Low. Recall number: D-1513-2020.