Maximum Strength/Non-Drowsy Tussin DM Adult Maximum Strength — Class III drug recall D-1286-2014
Terminated recall by Aaron Industries Inc, reported 2014-05-07, distributed nationwide. Presence of Precipitate; white substance confirmed as Guaifenesin, an active ingredient was observed in some b
| Recall number | D-1286-2014 |
|---|---|
| Product type | Drug |
| Classification | Class III |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Aaron Industries Inc, Lynwood, CA, United States |
| Recall initiated | 2014-04-11 |
| Classified | 2014-04-29 |
| Reported by FDA | 2014-05-07 |
| Terminated | 2015-02-13 |
| Distributed | Nationwide (US) |
| Quantity | 108,792 bottles |
| UPC / GTIN / UDI-DI | 00015127024303, 00015127024310, 00070253579523, 00321130763581, 00341520339677, 00715256714044, 00840986024719, 00840986024726 |
| Lot numbers | 06/14, 08/15, 140423, 140494, 140530, 142396, 142413, 145460, 145461, 145959, 148820, 148931, 149396, 149995, 150208, 150422, 150599, 151023, 151071, 151072, 151337, 73762, 73768, 73831, 73832, 74163, 76414, 78222, 78440, 78441, 79819, 80030, 80969, 82053, 82606, 83032 |
Product
Maximum Strength/Non-Drowsy Tussin DM Adult Maximum Strength, Cough Cold, Dextromethorphan HBr, USP, 10 mg (Cough Suppressant) , Guaifenesin, USP, 200 mg (Expectorant), 4, 8 fl oz bottles , OTC only, labeled as A) CareOne 8 fl oz bottle, Distributed by American Sales Company, Lancaster, NY 14086, UPC 341520339677, B) Our Family 4 fl oz bottle, Distributed by Nash Finch Company, NFC Brands, MPLS, MN 55435, UPC 070253579523, C) Premier Value 4, 8 fl oz bottle, Distributed by Chain Drug Consortium, LLC., Boca Raton, FL 33431, 4 fl oz UPC 840986024719; 8 fl oz UPC 840986024726, NDC 68016-177-XX, D) Rexall 4 fl oz bottle, Packaged for Dolencorp, LLC, Goodlettsville, TN 37072, UPC 715256714044, E) Safeway 4 fl oz, Distributed by Safeway INC, Pleasanton, CA 94566-0009, UPC 321130763581; F) Select Brand 4, 8 fl oz, Distributed by Select Brand Distributers, Pine Bluff, AR 71603, 4 fl oz UPC 015127024303; 8 fl oz UPC 015127024310.
Reason for recall
Presence of Precipitate; white substance confirmed as Guaifenesin, an active ingredient was observed in some bottles.
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-1286-2014. 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.