Drug recall D-0964-2015

Class III Terminated reported Apr 29, 2015

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

Reason for recall

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

Lots and codes

Lot BD375 exp 06/2016; BD566, BD661 exp. 08/2016

Recall details

Recalling firm
Reckitt Benckiser LLC, Parsippany, NJ
Quantity
155 cases (2000 pouches of 2 tablets per case)
Distribution
Nationwide
Type
Voluntary: Firm initiated
Recall initiated
November 10, 2014
Terminated
March 30, 2018

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