1. Skip to navigation
  2. Skip to content
  3. Skip to sidebar

Consumer Affairs

Vicks Dayquil Liquicaps Recalled


December 22, 2009
Vicks Dayquil Cold & Flu Liquicaps are beint recalled by Procter & Gamble because they fail to meet the child-resistant closure requirement.

The recall includes about 700,000 packages.

The cold and flu medicine contains acetaminophen and is not in child-resistant packaging and lacks the statement, This Package for Households Without Young Children, as required by the Poison Prevention Packaging Act. This medicine could cause serious health problems or death to a child if several of the capsules are swallowed.

The recall involves Vicks Dayquil Cold & Flu 24-Count Bonus Pack Liquicaps. The medicine comes in orange packaging with the green Vicks symbol and has the following UPC#: 3 23900 01087 1. No other Vicks product is included in this recall.

The liquicaps were sold at drug stores, grocery stores and other retailers nationwide between September 2008 and December 2009 for about $5. They were made in Canada.

Consumers should keep this product out of the reach of children. Consumers who purchased the product with the expectation that it would be in child-resistant packaging can contact Procter & Gamble for a full refund or a replacement coupon. Adult consumers can continue to use the product as directed.

For additional information, contact Procter & Gamble at (800) 251-3374 between 9 a.m. and 6 p.m. ET Monday through Friday or log on to their Web site at www.vicks.com.

The recall is being conducted in cooperation with the U.S. Consumer Product Safety Commission (CPSC).

Quantcast