Reckitt Benckiser LLC recalls Mucinex DM (guaifenesin 600mg and dextromethorphan HBr 30mg), extended-release bi-layer tablets, 2 tablets per pouch (N…

Recall date

November 10, 2014

Source

U.S. Food & Drug Administration (FDA) — enforcement report

Recall number

D-0964-2015

FDA classification

Class III

Brand / firm

Reckitt Benckiser LLC

Sold / distributed

Nationwide

Why it was recalled

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

Class III means the product violates regulations but is not likely to cause harm.

What was recalled

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