# FDA recall D-1097-2014

> **Aaron Industries Inc** · Class III · drug recall initiated 2014-02-04.

## Product

Tussin CF Adult Maximum Strength Multi-Symptom Cold liquid (dextromethorphan HBr 10 mg, guaifenesin 200 mg, phenylephrine HCl 5 mg) per 5 mL, 8 FL OZ (237 mL) bottle, Distributed by: Wal-Mart Stores, Inc., Bentonville, AR  72716, NDC 49035-229-08, UPC 6 81131 03884 3.

## Reason for recall

Presence of Precipitate: Recall is due to complaints of a white substance, confirmed as Guaifenesin, an active ingredient in the product which is precipitating out.

## Distribution

Nationwide

## Key facts

- **Recall number:** D-1097-2014
- **Recalling firm:** Aaron Industries Inc
- **Classification:** Class III
- **Product type:** drug
- **Status:** Terminated
- **Initiation date:** 2014-02-04
- **Report date:** 2014-03-12
- **Termination date:** 2014-10-29

- **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-1097-2014

## Citation

> AI Analytics. FDA recall D-1097-2014. Retrieved 2026-05-26 from https://api.ai-analytics.org/recall/D-1097-2014. Source: US FDA. Licensed CC0.

---

*[Dataset catalog](/datasets/) · [FDA recalls dataset](/datasets/fda-recalls) · CC0 1.0*