Drug recall D-1097-2014

Class III Terminated reported Mar 12, 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

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