Liquid vitamins for infants and children are among several supplements and drugs that the U.S. Food and Drug Administration is advising consumers and health care professionals not to use due to risk of severe infection.
The FDA is advising against using any liquid drug or dietary supplement products manufactured by PharmaTech LLC of Davie, Florida, and labeled by Rugby Laboratories, Major Pharmaceuticals and Leader Brands, due to potential contamination with the bacteria Burkholderia cepacia (B. cepacia) and the risk for severe patient infection.
The drug and dietary supplement products made by PharmaTech include liquid docusate sodium drugs (stool softeners), as well as various dietary supplements including liquid vitamin D drops and liquid multivitamins marketed for infants and children. A lab test done by the Centers for Disease Control and Prevention (CDC) found a strain of B. cepacia in samples of the stool softeners.
“B. cepacia poses a serious threat to vulnerable patients, including infants and young children who still have developing immune systems,” said FDA Commissioner Dr. Scott Gottlieb. “These products were distributed nationwide to retailers, health care facilities, pharmacies and sold online — making it important that parents,…