PlainRecalls
FDA Drug Low Class III Terminated

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

Reported: April 29, 2015 Initiated: November 10, 2014 #D-0964-2015

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

Reason for Recall

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

Details

Recalling Firm
Reckitt Benckiser LLC
Units Affected
155 cases (2000 pouches of 2 tablets per case)
Distribution
Nationwide
Location
Parsippany, NJ

Frequently Asked Questions

What product 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. Recalled by Reckitt Benckiser LLC. Units affected: 155 cases (2000 pouches of 2 tablets per case).
Why was this product recalled?
Defective container: A customer complaint revealed the presence of a defective seal on the top of a Mucinex pouch
Which agency issued this recall?
This recall was issued by the FDA Drug on April 29, 2015. Severity: Low. Recall number: D-0964-2015.