# FDA recall D-0787-2022

> **AptaPharma Inc.** · Class III · drug recall initiated 2022-03-29.

## Product

Wal-Tussin DM (dextromethorphan HBr/Guaifenesin), 12 FL OZ (354 mL) bottles, Distributed By: Walgreen Co. 200 Wilmot Rd., Deerfield, IL 60015, NDC 0363-0324-28.

## Reason for recall

Incorrect/Undeclared Excipient: Product contains alcohol

## Distribution

IL only

## Key facts

- **Recall number:** D-0787-2022
- **Recalling firm:** AptaPharma Inc.
- **Classification:** Class III
- **Product type:** drug
- **Status:** Terminated
- **Initiation date:** 2022-03-29
- **Report date:** 2022-05-04
- **Termination date:** 2024-04-24

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

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=D-0787-2022

## Citation

> AI Analytics. FDA recall D-0787-2022. Retrieved 2026-06-02 from https://api.ai-analytics.org/recall/D-0787-2022. Source: US FDA. Licensed CC0.

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