Tussin CF Adult Maximum Strength Multi-Symptom Cold liquid — Class III drug recall D-1097-2014
Terminated recall by Aaron Industries Inc, reported 2014-03-12, distributed nationwide. Presence of Precipitate: Recall is due to complaints of a white substance, confirmed as Guaifenesin, an active
| Recall number | D-1097-2014 |
|---|---|
| Product type | Drug |
| Classification | Class III |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Aaron Industries Inc, Lynwood, CA, United States |
| Recall initiated | 2014-02-04 |
| Classified | 2014-02-28 |
| Reported by FDA | 2014-03-12 |
| Terminated | 2014-10-29 |
| Distributed | Nationwide (US) |
| Quantity | 43,921 bottles |
| UPC / GTIN / UDI-DI | 00681131038843 |
| NDC | 49035-0229-08 |
| Lot numbers | 10/15, 11/15, 151631, 152767 |
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.
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-1097-2014. 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.