RecallDepth
Class III Terminated

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.

This recall has been terminated (originally issued March 12, 2014).

Company
Aaron Industries Inc
Recall Initiated
February 4, 2014
Posted
March 12, 2014
Recall Number
D-1097-2014
Voluntary / Mandated
Voluntary: Firm initiated
Quantity
43,921 bottles
Firm Location
Lynwood, CA, United States
Official Source
View on FDA website ↗

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

Nationwide

Lot / Code Info

Lot #: 151631, Exp 10/15 and 152767, Exp 11/15

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