FDAFDA · Food and drugs·Recall number D-1097-2014
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.
Published March 12, 2014 · Recall initiated: February 4, 2014
Status when published: Terminated — openFDA updates weekly, so this field may not reflect the current status. Always confirm with the official notice.
What's the hazard
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.
What to do
Voluntary: Firm initiated · Telephone
Recall details
- Manufacturer
- Aaron Industries Inc
- Distributor
- Nationwide
- Lot
- Lot #: 151631, Exp 10/15 and 152767, Exp 11/15
- Risk classification
- Class III
- Area (FDA)
- drug
- Country
- United States
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