# FDA recall D-0964-2015

> **Reckitt Benckiser LLC** · Class III · drug recall initiated 2014-11-10.

## 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

## Distribution

Nationwide

## Key facts

- **Recall number:** D-0964-2015
- **Recalling firm:** Reckitt Benckiser LLC
- **Classification:** Class III
- **Product type:** drug
- **Status:** Terminated
- **Initiation date:** 2014-11-10
- **Report date:** 2015-04-29
- **Termination date:** 2018-03-30

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Parsippany, NJ, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=D-0964-2015

## Citation

> AI Analytics. FDA recall D-0964-2015. Retrieved 2026-05-29 from https://api.ai-analytics.org/recall/D-0964-2015. Source: US FDA. Licensed CC0.

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