Drug recall
Tylenol Cold Multi Symptom Daytime Liquid, (acetaminophen 325mg, dextromethorphan HBr 10mg and phenylephrine…
FDA recall event 57324 · Class III · Mcneil Consumer Healthcare, Div Of Mcneil-ppc, Inc.
Key facts
| Event ID | 57324 |
|---|---|
| Recall numbers | D-207-2011, D-208-2011, D-209-2011 |
| Recalling firm | Mcneil Consumer Healthcare, Div Of Mcneil-ppc, Inc. |
| Product type | Drugs |
| Products | Tylenol Cold Multi Symptom Daytime Liquid, (acetaminophen 325mg, dextromethorphan HBr 10mg and phenylephrine 5mg), 8 oz bottles, Citrus Burst flavor, Distributed by McNeil Consumer Healthcare…, Tylenol Cold Multi Symptom Nighttime Liquid, (acetaminophen 325mg, dextromethorphan HBr 10mg, doxylamine succinate 6.25mg and phenylephrine 5mg), 8 oz bottles, Cool Burst flavor, Distributed by McNeil…, Tylenol Cold Multi Symptom Severe Day Liquid (acetaminophen 325mg, dextromethorphan HBr 10mg, guaifenesin 200mg and phenylephrine 5mg), 8 oz Cool Burst, Distributed by McNeil Consumer Healthcare… |
| Classification | Class III |
| Status | Terminated |
| Voluntary or mandated | Firm Initiated |
| Reason for recall | Misbranded: alcohol content not listed on front panel, Misbranded; alcohol content not listed on front panel |
| Initiation date | Nov 23, 2010 |
| Termination date | Apr 11, 2013 |
| City | Fort Washington |
| State | PA |
| Country | United States |
| FEI number | 2510184 |
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