Drug recall D-1097-2014
Product
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.
Reason for recall
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.
Lots and codes
Lot #: 151631, Exp 10/15 and 152767, Exp 11/15
Recall details
- Recalling firm
- Aaron Industries Inc, Lynwood, CA
- Quantity
- 43,921 bottles
- Distribution
- Nationwide
- Type
- Voluntary: Firm initiated
- Recall initiated
- February 4, 2014
- Terminated
- October 29, 2014
Related products
- NDC 49035-229 Acne Treatment · Benzoyl Peroxide 100 mg/g · Walmart Inc.