Low risk — use of or exposure to this product is not likely to cause adverse health consequences.
Rite Aid Maximum Strength Tussin Cough & Cold Mucus Relief CF Recalled by Aaron Industries Inc Due to Presence of Precipitate; white substance confirmed as Guaifenesin,...
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
Rite Aid Maximum Strength Tussin Cough & Cold Mucus Relief CF, (dextromethorphan HBr 10 mg, guaifenesin 200 mg, phenylephrine HCI 5 mg, 4 FL. OZ./12 PK (UPC Code: 0-11822-57307-8) and 8 FL.OZ./12 PK (UPC Code: 0-11822-57313-9), Distributed by: Rite Aid, Camp Hill, PA, 17011
Quantity: 35,652 bottles (2,971 cases)
Why Was This Recalled?
Presence of Precipitate; white substance confirmed as Guaifenesin, an active ingredient was observed in some bottles. If the product is shaken or warmed the white particles goes into the solution.
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