FDA Drug recall D-187-2013
Select Brand Cough Control CF Max, Maximum Strength for MUCUS RELIEF, (dextromethorphan HBr 10 mg, guaifenesin 200 mg, phenylephrine HCI 5…
- FDA Drug
- Class III
- terminated
- Published 2013-03-13
On 2013-03-13 the FDA classified a Class III recall of Select Brand Cough Control CF Max, Maximum Strength for MUCUS RELIEF, (dextromethorphan HBr 10 mg, guaifenesin 200 mg, phenylephrine HCI 5… by Aaron Industries, citing 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 i….
Read the official FDA Drug notice
| Agency | FDA Drug |
|---|---|
| Recall number | D-187-2013 |
| Classification | Class III |
| Status | terminated |
| Initiated | 2013-01-18 |
| Published | 2013-03-13 |
| Last updated | 2026-09-13 11:51 UTC |
| Company | Aaron Industries |
| Distribution | US |
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
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.
Identifiers
| upc | 015127025355 |
|---|---|
| code_info | Lot# 71648, 68088; FP-47-041-02535 |
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:51 UTC. Current status: terminated.
Source
Official record: https://api.fda.gov/drug/enforcement.json?search=recall_number:%22D-187-2013%22
RecallRadar indexes public recall notices from the FDA, USDA FSIS, and CPSC. The official agency notice is the authoritative source. Always confirm details at the linked source before acting.