Abbott has expanded the list of powdered infant formulas under recall
produced in Abbott’s Sturgis, Michigan, facility. A total of five hospitalizations have now been reported, with two deaths. Four of the babies were infected with cronobacter sakazakii bacteria, and one with salmonella. Both of the infants who died were infected with cronobacter sakazakii. The illnesses were reported in three states: one in Minnesota, two in Ohio, and two in Texas.
The most recent infant death is linked to Similac 60/40, a specialty formula that was not included in Abbott’s initial recall announced on February 17. The Similac PM 60/40 formula was distributed in the U.S. and Israel and is now also under recall. The Feb. 17 recall involves powdered Similac, Alimentum and Elecare powdered infant formulas. Liquid formula products are not impacted. These formulas were distributed across the U.S. and likely to other countries.The first two digits of the code are 22-37; andIn addition, as of Feb. 28:The FDA also reminds caregivers never to dilute infant formula or use homemade formula.
Consumers with product that meets the above criteria can either discard the formula or return it for a refund. Families who get formula through WIC should return the formula to the store for exchange or refund, or call 1-800-986-8540 for assistance.found several positive cronobacter sakazakii results from environmental samples. The FDA also found “adverse inspectional observations” at the facility.
“As this is a product used as the sole source of nutrition for many of our nation’s newborns and infants, the FDA is deeply concerned about these reports of bacterial infections,” says Frank Yiannas, FDA Deputy Commissioner for Food Policy and Response.
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