Class III โ€” Low Risk

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

Wal-Tussin DM (dextromethorphan HBr/Guaifenesin) Recalled by AptaPharma Inc. Due to Undeclared Excipient

Date: March 29, 2022
Company: AptaPharma Inc.
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 AptaPharma Inc. directly.

Affected Products

Wal-Tussin DM (dextromethorphan HBr/Guaifenesin), 12 FL OZ (354 mL) bottles, Distributed By: Walgreen Co. 200 Wilmot Rd., Deerfield, IL 60015, NDC 0363-0324-28.

Quantity: 40000 - 50000 units

Why Was This Recalled?

Incorrect/Undeclared Excipient: Product contains alcohol

Where Was This Sold?

This product was distributed to 1 state: IL

Affected (1 state)Not affected

About AptaPharma Inc.

AptaPharma Inc. has 1 total recall tracked by RecallDetector.

Related Recalls

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