• Decrease font size
  • Return font size to normal
  • Increase font size
U.S. Department of Health and Human Services

Enforcement Report - Week of August 7, 2013

  • Print
  • Share
  • E-mail
-

Product Detail

Product Description 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.
Recall Number D-827-2013
Classification Class II
Code Info Lot # 3051171961, Exp 09/14; Brand Code 84855363
Product Distributed Qty 35,568 cartons
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.

Event Detail

Event Id 65650
Product Type Drugs
Status Ongoing
Recalling Firm Procter & Gamble Co
City Mason
State OH
Country US
Voluntary / Mandated Voluntary: Firm Initiated
Recall Initiation Date 2013-07-03
Initial Firm Notification of Consignee or Public Letter
Distribution Pattern Nationwide
-
-