FDA announces infant formula recall

On Thursday, the U.S. Food and Drug Administration announced it is investigating consumer complaints of Cronobacter sakazakii and Salmonella Newport infections.
All of the cases are reported to have consumed powdered infant formula produced from Abbott Nutrition’s Sturgis, Michigan facility. Along with the Centers for Disease Control and Prevention and state and local partners, the FDA is alerting consumers to avoid purchasing or using certain powdered infant formula products produced at this facility.
Abbott is working with the FDA to initiate a voluntary recall of the potentially affected product.
The FDA is advising consumers not to use Similac, Alimentum, or EleCare powdered infant formulas if:
—The first two digits of the code are 22 through 37; and
—The code on the container contains K8, SH or Z2; and
—The expiration date is 4-1-2022 (APR 2022) or later.
For the full article on the recall, visit www.fda.gov/news-events/press-announcements/fda-warns-consumers-not-use-....