Select Brand Cough Control CF Max — Class III drug recall D-187-2013
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-187-2013 |
|---|---|
| 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) |
| UPC / GTIN / UDI-DI | 00015127025355 |
| NDC | 15127-0025-04 |
| Lot numbers | 68088, 71648, FP-47-041-02535 |
Product
Select Brand Cough Control CF Max, Maximum Strength for MUCUS RELIEF, (dextromethorphan HBr 10 mg, guaifenesin 200 mg, phenylephrine HCI 5 mg), 4 fl.oz 12pk (NDC 15127-025-04; UPC Code: 0-15127-02535-5), Distributed by: Select Brand Distributors, Pine Bluff, AR 71603 USA.
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-187-2013. 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.