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.