Drug recall
Maximum Strength/Non-Drowsy Tussin DM Adult Maximum Strength, Cough Cold, Dextromethorphan HBr, USP, 10 mg…
FDA recall event 68003 · Class III · Aaron Industries Inc
Key facts
| Event ID | 68003 |
|---|---|
| Recall numbers | D-1286-2014 |
| Recalling firm | Aaron Industries Inc |
| Product type | Drugs |
| Products | 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… |
| Classification | Class III |
| Status | Terminated |
| Voluntary or mandated | Firm Initiated |
| Reason for recall | Presence of Precipitate; white substance confirmed as Guaifenesin, an active ingredient was observed in some bottles. |
| Initiation date | Apr 11, 2014 |
| Report date | May 7, 2014 |
| Termination date | Feb 13, 2015 |
| City | Lynwood |
| State | CA |
| Country | United States |
| FEI number | 1000160562 |
At a glance
- 1–9 Products in this recall
- 10–99 FDA inspections of this firm (FEI)
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About FDA drug and product recalls
FDA enforcement reports list recalls of drugs, biologics, foods and other FDA-regulated products, classified by the potential health hazard.
Source: U.S. Food and Drug Administration (FDA), Enforcement Reports · Source date: