A baby formula plant recall resulting from infant illnesses and deaths may have been caught earlier, according to Food and Drug Administration ( FDA ) records. On February 17 of this year, Abbott initiated a voluntary recall of its powder baby formulas, for brands including Similac, Alimentum and EleCare, that were manufactured at one of the company’s manufacturing facilities in Sturgis, Michigan. The recall was due to the presence of Cronobacter sakazakii — a rare bacteria the Centers for Disease and Control and Prevention ( CDC ) says has been found in powdered infant formula , skimmed milk powder, herbal teas and starches, and is “lethal for infants and can be serious among people with immunocompromising conditions and the elderly.” Abbott initially received four bacteria-related complaints from individuals whose children had consumed powder manufactured in the facility, in addition to potential claims of salmonella. The FDA reported that five infants, all of whom had consumed the recalled formula, contracted either Cronobacter or salmonella—potentially leading to the deaths of at least two, according to CBS News. Abbott said quality testing for Cronobacter and other pathogens in their facilities is routine. Cronobacter was found in the plant in a non-product area, though… Read full this story
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