
Click to enlarge image
US/Silver Spring: Abbott Nutrition Products, an Abbott Park, Illinois establishment, recalls expands its existing recall for certain batch/lots of Alimentum, EleCare and Similac Infant Formula manufactured in Sturgis, Michigan, one of the company’s manufacturing facilities, from the American marketplace to include an additional batch/lot of Similac PM Infant Formula.
The initial recall was initiated due to possible Cronobacter sakazakii and Salmonella contamination and consequential risks of Gram-negative bacterial infection, severe illness and/or possible life-changing complications, all serious health and safety hazards requiring immediate medical intervention to minimize pain and suffering as well as prevent life-altering injury or death.
FDA: http://ht.ly/QpUn30scSPn
Direct link: https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/abbott-voluntarily-expands-recall-powder-formulas-manufactured-one-plant
Additional information:
The US Food and Drug Administration (“FDA”) reports the following Infant Formula products are subject to this recall:
Continue reading →
Like this:
Like Loading...
Filed under: Bacterial or viral contamination, Food & Drink, Salmonella [Gram-neg], US FDA | Tagged: Abbott Laboratories Co., Abbott Nutrition Products, Abbott Nutrition Products or Abbott Laboratories Co., Alimentum, baby formula, bacterial contamination hazard, Cronobacter sakazakii, EleCare, FDA, infant formula, Recalls Direct RIN: 15561-2022, Salmonella hazard, Salmonella poisoning hazard, Salmonellosis hazard, Similac, Similac PM 60/40, suspected Salmonella contamination, US FDA, US Food and Drug Administration | Leave a comment »