Wal-Tussin DM recalled over undeclared excipient
- Recall date
- March 29, 2022
- Source
- U.S. Food & Drug Administration (FDA) — enforcement report
- Official notice title
- AptaPharma Inc. recalls Wal-Tussin DM (dextromethorphan HBr/Guaifenesin), 12 FL OZ (354 mL) bottles, Distributed By: Walgreen Co. 200 Wilmot Rd…
- Recall number
- D-0787-2022
- FDA classification
- Class III
- Brand / firm
- AptaPharma Inc.
- Sold / distributed
- IL only
Why it was recalled
Incorrect/Undeclared Excipient: Product contains alcohol
Class III means the product violates regulations but is not likely to cause harm.
What was recalled
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.
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