# FDA recall D-827-2013

> **Procter & Gamble Co** · Class II · drug recall initiated 2013-07-03.

## Product

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 phenylephrine HCl 5 mg) liquicaps Combopack, each 48-count liquicaps per carton contains 32 DayQuil Sinex DayTime Liquicaps and 16 NyQuil Sinex NightTime Liquicaps per carton, Made In Canada, Dist. by Procter & Gamble, Cincinnati, OH 45202, UPC 3 23900 01454 1.

## 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.

## Distribution

Nationwide

## Key facts

- **Recall number:** D-827-2013
- **Recalling firm:** Procter & Gamble Co
- **Classification:** Class II
- **Product type:** drug
- **Status:** Terminated
- **Initiation date:** 2013-07-03
- **Report date:** 2013-08-07
- **Termination date:** 2014-10-08

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Mason, OH, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=D-827-2013

## Citation

> AI Analytics. FDA recall D-827-2013. Retrieved 2026-06-23 from https://api.ai-analytics.org/recall/D-827-2013. Source: US FDA. Licensed CC0.

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