drugs Class III Updated 2015-04-29

Reckitt Benckiser LLC recalls Mucinex DM (guaifenesin 600mg and dextromethorphan HBr 30mg)

Recalled Product

Mucinex DM (guaifenesin 600mg and dextromethorphan HBr 30mg), extended-release bi-layer tablets, 2 tablets per pouch (NDC 63824-056-72), OTC, Distributed by Reckitt Benckiser, Parsippany, NJ 07054-0224 Made in England

Hazard / Issue

Defective container: A customer complaint revealed the presence of a defective seal on the top of a Mucinex pouch

Issued by

FDA

Distribution: Nationwide (United States)
Lot/Code Info: Lot BD375 exp 06/2016; BD566, BD661 exp. 08/2016
View official government recall

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