Low risk — use of or exposure to this product is not likely to cause adverse health consequences.
Tussin CF Adult Maximum Strength Multi-Symptom Cold liquid (dextromethorphan HBr Recalled by Aaron Industries Inc Due to Presence of Precipitate: Recall is due to complaints...
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 Aaron Industries Inc directly.
Affected Products
Tussin CF Adult Maximum Strength Multi-Symptom Cold liquid (dextromethorphan HBr 10 mg, guaifenesin 200 mg, phenylephrine HCl 5 mg) per 5 mL, 8 FL OZ (237 mL) bottle, Distributed by: Wal-Mart Stores, Inc., Bentonville, AR 72716, NDC 49035-229-08, UPC 6 81131 03884 3.
Quantity: 43,921 bottles
Why Was This Recalled?
Presence of Precipitate: Recall is due to complaints of a white substance, confirmed as Guaifenesin, an active ingredient in the product which is precipitating out.
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About Aaron Industries Inc
Aaron Industries Inc has 7 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Drug). Last updated March 26, 2026. View original report