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.
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