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Recall data is sourced from official U.S. government agencies (CPSC, FDA, NHTSA, USDA) and processed using AI to improve readability. This site is not affiliated with or endorsed by any government agency. Always refer to the original agency notice for authoritative information.

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Low RiskFDA Drug
Medications & Supplements/Over-the-Counter

Walgreens Wal-Tussin DM Cough Syrup Recalled for Undeclared Alcohol

Agency Publication Date: April 25, 2022
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Summary

AptaPharma Inc. has recalled Wal-Tussin DM (dextromethorphan HBr/Guaifenesin) cough syrup, sold in 12 FL OZ (354 mL) bottles, because the product contains alcohol that is not listed on the label. Between 40,000 and 50,000 units are affected, and the recall covers all lots of the product distributed exclusively to Walgreens locations in Illinois. No incidents or injuries have been reported to date regarding this issue.

Risk

The product contains undeclared alcohol, which can cause adverse health effects for individuals who must avoid alcohol due to medical conditions, religious reasons, or interactions with other medications.

What You Should Do

  1. The recalled product is Wal-Tussin DM (dextromethorphan HBr/Guaifenesin) cough syrup sold in 12 FL OZ (354 mL) bottles with NDC 0363-0324-28 and includes all lots.
  2. If you have health concerns, contact your healthcare provider or pharmacist. Return any unused product to the place of purchase for a refund, throw it away, or contact AptaPharma Inc. for further instructions.
  3. Call the FDA Consumer Complaint hotline at 1-888-723-3332 (1-888-SAFEFDA) or visit www.fda.gov/safety/recalls for additional questions.

Your Remedy Options

You have 2 options:

๐Ÿ’ฐOption 1: Full Refund
How to: Contact your healthcare provider or pharmacist for guidance, or return any unused product to the place of purchase for a refund
๐Ÿ—‘๏ธOption 2: Dispose of Product
How to: Throw the product away. For prescription medications, a DEA take-back location or pharmacy mail-back program is preferred when available.

Affected Products

Product: Wal-Tussin DM (dextromethorphan HBr/Guaifenesin) (12 FL OZ)by Walgreens
Variants: Cough Syrup
Lot Numbers:
All lots
NDC:
0363-0324-28

Recall #: D-0787-2022. Distributed By: Walgreen Co. 200 Wilmot Rd., Deerfield, IL 60015.

Additional Information

Agency: Food and Drug Administration (FDA)
Event ID: 89905
Status: Resolved
Manufacturer: AptaPharma Inc.
Sold By: Walgreens; Walgreen Co.
Manufactured In: United States
Units Affected: 40000 - 50000 units
Distributed To: Illinois

AI-Enhanced Content: The summary, action steps, and risk assessment on this page were generated by AI from official government recall data to improve readability. This is not legal or medical advice. Always refer to the official agency sources below for authoritative information.

Sources: FDA iRES ยท Raw API Response

openFDA Disclaimer: This recall information is sourced from the openFDA API. Do not rely on openFDA to make decisions regarding medical care. While we make every effort to ensure that data is accurate, you should assume all results are unvalidated. Refer to the openFDA terms of service for more information.