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Vicks Dayquil Cold & Flu Liquicaps Recalled by Procter & Gamble Due To Failure to Meet Child-Resistant Closure Requirement

U.S. CPSCChemicalIngestionDec 18, 2009
Photo from the official notice: Vicks Dayquil Cold & Flu Liquicaps Recalled by Procter & Gamble Due To Failure to Meet Child-Resistant Closure Requirement

Photos from the official notice: U.S. Consumer Product Safety Commission · image rights

Hazard

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.

Remedy

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.

Replace, Refund

Incidents & injuries

None reported.

Product description

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 Vick's product is included in this recall.

Sold on

Drug stores, grocery stores and other retailers nationwide between September 2008 and December 2009 for about $5.

Contact the company

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

What should I do?

Stop using the product and follow the remedy below. Contact the company for a refund, repair or replacement — recall remedies are free.

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