FDA Drug recall D-419-2013
Rite Aid brand Maximum Strength Tussin Cough & Cold Mucus Relief CF, (dextromethorphan HBr 10 mg, guaifenesin 200 mg and phenylephrine HCl…
- FDA Drug
- Class III
- terminated
- Published 2013-05-29
On 2013-05-29 the FDA classified a Class III recall of Rite Aid brand Maximum Strength Tussin Cough & Cold Mucus Relief CF, (dextromethorphan HBr 10 mg, guaifenesin 200 mg and phenylephrine HCl… 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-419-2013 |
| Classification | Class III |
| Status | terminated |
| Initiated | 2013-04-04 |
| Published | 2013-05-29 |
| Last updated | 2026-09-13 11:51 UTC |
| Company | Aaron Industries |
| Distribution | US |
Product
Rite Aid brand Maximum Strength Tussin Cough & Cold Mucus Relief CF, (dextromethorphan HBr 10 mg, guaifenesin 200 mg and phenylephrine HCl 5 mg), 4 oz. package size, Distributed by: Rite Aid, Camp Hill, PA --- UPC Code: 0 11822 57307 8.
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 | 011822573078 |
|---|---|
| code_info | Lot # 82507 and 82720. |
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-419-2013%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.