D-1097-2014 Class III Terminated
Recall Details
- Product Type
- Drugs
- Report Date
- March 12, 2014
- Initiation Date
- February 4, 2014
- Termination Date
- October 29, 2014
- Voluntary/Mandated
- Voluntary: Firm initiated
- Product Quantity
- 43,921 bottles
Product Description
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.
Distribution Pattern
Nationwide
Code Information
Lot #: 151631, Exp 10/15 and 152767, Exp 11/15