US Drug Recall Register
Class III · Low risk Ongoing Initiated Sep 25, 2024 (2 years ago)

Adult Cough and Chest Congestion (Dextromethorphan HBr USP 20 mg, Guaifenesin USP…

Class III — Low risk. Unlikely to cause harm, but violates FDA regulations.

Why it was recalled

Crystallization: Lack of uniformity - a change in texture, chunky, grainy, and small crystal substances inside the bottles.

What was recalled

Adult Cough and Chest Congestion (Dextromethorphan HBr USP 20 mg, Guaifenesin USP 400mg), packaged in 4 oz bottles further package in cartons, Distributed by: Genexa Inc., Alanta, GA, 30318, NDC-69676-0077-9, UPC Code # 850015736155

Recalling firm
Denison Pharmaceuticals, LLC
Origin
RI, United States
Initiated by
Voluntary: Firm initiated
FDA recall number
D-0033-2025

What should you do? A recall doesn't always mean your specific bottle is affected - it often applies to certain lots only. Check the lot number on your package against the FDA notice, and talk to your pharmacist before stopping any medication.

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