DayQuil Sinex DayTime Sinus Relief — Class II drug recall D-827-2013
Terminated recall by Procter & Gamble Co, reported 2013-08-07, distributed nationwide. Unit Dose Mispackaging: Product packaging defect which could result in code date smearing, incomplete blister
| Recall number | D-827-2013 |
|---|---|
| Product type | Drug |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Procter & Gamble Co, Mason, OH, United States |
| Recall initiated | 2013-07-03 |
| Classified | 2013-07-26 |
| Reported by FDA | 2013-08-07 |
| Terminated | 2014-10-08 |
| Distributed | Nationwide (US) |
| Quantity | 35,568 cartons |
| Reason classes | packaging |
| UPC / GTIN / UDI-DI | 00323900014541 |
| Lot numbers | 09/14, 3051171961 |
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.
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-827-2013. 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.