RB Mucinex Voluntary Recall

For Immediate Release

April 24, 2015; 4:00pm

DPHSS Release No. 2015-033

RB Mucinex Voluntary Recall

The Department of Public Health and Social Services, in coordination with the U.S. Food & Drug Administration, would like to inform the public of a voluntary recall involving RB MUCINEX FAST-MAX bottles may not have the correct corresponding drug facts label on the back.  

The mislabeled recalled item could cause the consumer to be unaware of the side effects and/or risks associated when ingesting the product and its ingredients, including Acetaminophen, Dextromethorphan, Guaifenesin, Phenylephrine, and/or Diphenhydramine. 

To date, the Division of Environmental Health has determined that the implicated products were sold at K Mart.  All affected products have been removed from the retail sales floor. 

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