Drug recall
DayQuil Sinex DayTime Sinus Relief (acetaminophen 325 mg and phenylephrine HCl 5 mg) liquicaps and NyQuil…
FDA recall event 65650 · Class II · Procter & Gamble Co
Key facts
| Event ID | 65650 |
|---|---|
| Recall numbers | D-827-2013 |
| Recalling firm | Procter & Gamble Co |
| Product type | Drugs |
| Products | DayQuil Sinex DayTime Sinus Relief (acetaminophen 325 mg and phenylephrine HCl 5 mg) liquicaps and NyQuil Sinex NightTime Sinus Relief (acetaminophen 325 mg, doxylamine succinate 6.25 mg, and… |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Firm Initiated |
| Reason for recall | Unit Dose Mispackaging: Product packaging defect which could result in code date smearing, incomplete blister card cuts, and missing or incorrectly placed liquicaps within the blisters. |
| Initiation date | Jul 3, 2013 |
| Report date | Aug 7, 2013 |
| Termination date | Oct 8, 2014 |
| City | Mason |
| State | OH |
| Country | United States |
| FEI number | 3000719926 |
At a glance
- 1–9 Products in this recall
- 1–9 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: