FDA recall record

Mucinex DM recall — FDA D-0964-2015

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

Class IIIclassification
D-0964-2015official record ID
Apr 29, 2015report date

Recall record at a glance

Official recordD-0964-2015
CategoryDrug Recalls
ClassificationClass III
FDA record statusTerminated
Recalling firmReckitt Benckiser LLC
Report dateApr 29, 2015
Recall initiation dateNov 10, 2014
Quantity155 cases (2000 pouches of 2 tablets per case)
LocationParsippany, NJ, United States

Official product description

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

Why the product was recalled

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

Distribution information

Nationwide

How to read the classification

FDA Class III generally covers situations in which use of or exposure to the product is not likely to cause adverse health consequences. The classification displayed here is taken from the FDA enforcement record.

Additional record details

Recall type: Voluntary: Firm initiated. Initial notification: Letter.

What to do next

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About this record

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