# FDA recall D-188-2013

> **Aaron Industries Inc** · Class III · drug recall initiated 2013-01-18.

## Product

Wal-Mart Equate Tussin CF Adult Maximum Strength, Multi-Symptom Cold, (dextromethorphan HBr 10 mg, guaifenesin 200 mg, phenylephrine HCI 5 mg), 8 FL OZ (235 mL) (NDC 49035-229-08; UPC Code: 6-81131-03884-30), Distributed by: Wal-Mart Stores, Inc., Bentonville, AR 72712.

## Reason for recall

Presence of Precipitate; white substance confirmed as Guaifenesin, an active ingredient was observed in some bottles.  If the product is shaken or warmed the white particles goes into the solution.

## Distribution

Nationwide

## Key facts

- **Recall number:** D-188-2013
- **Recalling firm:** Aaron Industries Inc
- **Classification:** Class III
- **Product type:** drug
- **Status:** Terminated
- **Initiation date:** 2013-01-18
- **Report date:** 2013-03-13
- **Termination date:** 2013-11-01

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Lynwood, CA, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=D-188-2013

## Citation

> AI Analytics. FDA recall D-188-2013. Retrieved 2026-05-27 from https://api.ai-analytics.org/recall/D-188-2013. Source: US FDA. Licensed CC0.

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