Wal-Tussin DM — Class III drug recall D-0787-2022
Terminated recall by AptaPharma Inc., reported 2022-05-04, distributed in IL. Incorrect/Undeclared Excipient: Product contains alcohol
| Recall number | D-0787-2022 |
|---|---|
| Product type | Drug |
| Classification | Class III |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | AptaPharma Inc., Pennsauken, NJ, United States |
| Recall initiated | 2022-03-29 |
| Classified | 2022-04-25 |
| Reported by FDA | 2022-05-04 |
| Terminated | 2024-04-24 |
| Distributed | IL |
| Reason classes | undeclared allergen |
| NDC | 00363-0324-28 |
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
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/D-0787-2022. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.