# FDA recall D-419-2013

> **Aaron Industries Inc** · Class III · drug recall initiated 2013-04-04.

## Product

Rite Aid brand Maximum Strength Tussin Cough & Cold Mucus Relief CF, (dextromethorphan HBr 10 mg, guaifenesin 200 mg and phenylephrine HCl 5 mg), 4 oz. package size, Distributed by: Rite Aid, Camp Hill, PA --- UPC Code: 0 11822 57307 8.

## 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 in the US: MD, MI, AL, NC, CT, NY, PA, OR, WV.

## Key facts

- **Recall number:** D-419-2013
- **Recalling firm:** Aaron Industries Inc
- **Classification:** Class III
- **Product type:** drug
- **Status:** Terminated
- **Initiation date:** 2013-04-04
- **Report date:** 2013-05-29
- **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-419-2013

## Citation

> AI Analytics. FDA recall D-419-2013. Retrieved 2026-05-26 from https://api.ai-analytics.org/recall/D-419-2013. Source: US FDA. Licensed CC0.

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