Well at Walgreens Wal-Tussin CF Max — Class III drug recall D-185-2013
Terminated recall by Aaron Industries Inc, reported 2013-03-13, distributed nationwide. Presence of Precipitate; white substance confirmed as Guaifenesin, an active ingredient was observed in some b
| Recall number | D-185-2013 |
|---|---|
| Product type | Drug |
| Classification | Class III |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Aaron Industries Inc, Lynwood, CA, United States |
| Recall initiated | 2013-01-18 |
| Classified | 2013-03-07 |
| Reported by FDA | 2013-03-13 |
| Terminated | 2013-11-01 |
| Distributed | Nationwide (US) |
| NDC | 00363-0229-08 |
| Lot numbers | 80798, FP-49-081-14870 |
Product
Well at Walgreens Wal-Tussin CF Max, MAXIMUM STRENGTH ADULT NON-DROWSY, Multi-Symptom Cold, (dextromethorphan HBr 10 mg, guaifenesin 200 mg, phenylephrine HCI 5 mg), 8 FL OZ (237 mL) bottles, Distributed by: Walgreen Co, Deerfield, IL 60015 ---- NDC 0363-0229-08
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.
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-185-2013. 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.