Reported Mar 12, 2014 · Terminated
Tussin CF Adult Maximum Strength Multi-Symptom Cold liquid (dextromethorphan HBr 10 mg, guaifenesin 200 mg,…
Aaron Industries Inc.
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.What you should do
Stop using the affected lot and contact the recalling firm for the return or refund process. Check the FDA enforcement report for lot-level detail.
Firm contact: Aaron Industries Inc · 11865 Alameda St · Lynwood, CA · 90262-4022
Is this the product you have?
- 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 byWal-Mart Stores, Inc., Bentonville, AR 72716, NDC 49035-229-08, UPC 6 81131 03884 3
- Lot codes and dates
Lot #: 151631Exp 10/15 and 152767Exp 11/15
- Amount recalled
- 43,921 bottles
Where it was sold
- Nationwide
Why it was recalled
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.
This product is unlikely to cause harm, but it breaks a safety or labelling rule.
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