PlainRecalls
FDA Drug Low Class III Terminated

Rite Aid brand Maximum Strength Tussin Cough & Cold Mucus Relief CF, (dextromethorphan HBr 10 mg, guaifenesin 200 mg and phenylephrine HCl 5 mg), 4 oz. package size, Distributed by: Rite Aid, Camp Hill, PA --- UPC Code: 0 11822 57307 8.

Reported: May 29, 2013 Initiated: April 4, 2013 #D-419-2013

Product Description

Rite Aid brand Maximum Strength Tussin Cough & Cold Mucus Relief CF, (dextromethorphan HBr 10 mg, guaifenesin 200 mg and phenylephrine HCl 5 mg), 4 oz. package size, Distributed by: Rite Aid, Camp Hill, PA --- UPC Code: 0 11822 57307 8.

Reason for Recall

Presence of Precipitate; white substance confirmed as Guaifenesin, an active ingredient was observed in some bottles. If the product is shaken or warmed the white particles goes into the solution.

Details

Recalling Firm
Aaron Industries Inc
Units Affected
27,144 bottles
Distribution
Nationwide in the US: MD, MI, AL, NC, CT, NY, PA, OR, WV.
Location
Lynwood, CA

Frequently Asked Questions

What product was recalled?
Rite Aid brand Maximum Strength Tussin Cough & Cold Mucus Relief CF, (dextromethorphan HBr 10 mg, guaifenesin 200 mg and phenylephrine HCl 5 mg), 4 oz. package size, Distributed by: Rite Aid, Camp Hill, PA --- UPC Code: 0 11822 57307 8.. Recalled by Aaron Industries Inc. Units affected: 27,144 bottles.
Why was this product recalled?
Presence of Precipitate; white substance confirmed as Guaifenesin, an active ingredient was observed in some bottles. If the product is shaken or warmed the white particles goes into the solution.
Which agency issued this recall?
This recall was issued by the FDA Drug on May 29, 2013. Severity: Low. Recall number: D-419-2013.