Total Adverse Events: 5 (4 Cronobacter, 1 Salmonella)
Hospitalizations: 5
Reported Deaths: 2
Adverse Event Dates: 9/16/2021 – 1/4/2022
States with Adverse Events: MN (1), OH (2), TX (2)
Product Distribution: Nationwide and International

The FDA, along with CDC and state and local partners are investigating consumer complaints and/or reports of infant illness related to

Enterobacter sakazakii- E. sakazakii infections have been reported in a variety of locations over the past several years among infants fed milk-based powdered infant formula products from various manufacturers.

On February 10, 2022, CDC was notified of FDA’s investigation of consumer complaints of infant illness related to products from Abbott Nutrition

This is a new reported illnesses. The FDA had been investigating complaints of four infant illnesses from three states – Ohio, Minnesota and Texas.  All four cases related to these complaints were hospitalized and Cronobacter may have contributed to a death in one case.

The West Virginia Department of Health and Human Resources (DHHR), Bureau

Vadilal Industries (USA) Inc. of Newark, NJ is voluntarily recalling two batches of frozen Custard Apple Pulp because it has the potential to be contaminated with Salmonella, an organism which can cause serious and sometimes fatal infections in young children, frail or elderly people, and others with weakened immune systems. Healthy persons infected with

2008 Powdered Infant Formula – Cronobacter sakazakii

Powdered infant formula is not sterile and has been implicated in Cronobacter outbreaks. Cronobacter is a rare cause of infant blood infections and meningitis; it carries a 40% mortality rate. Two infants, in New Mexico, who were not related to one another, and lived 200 miles apart, developed

The table below shows information about four other ongoing outbreak investigations being managed by FDA’s CORE Response Teams and one investigation that has been closed. The investigations are in a variety of stages. Some outbreaks have limited information with active investigations ongoing, others may be near completion. The table below has been abbreviated to show

One ill with Salmonella, Three ill with Cronobacter sakazakii with one death in Minnesota, Ohio and Texas

FDA: Findings to date include several positive Cronobacter results from environmental samples taken by FDA at Abbott in Sturgis, Michigan facility.

FDA: A review of the Abbott ’s internal records also indicate environmental contamination with Cronobacter sakazakii.

FDA:

Around 50 percent of infants who have an Cronobacter sakazakii die.

Cronobacter sakazakii is a bacterium that causes a rare but often fatal infection of the bloodstream and central nervous system. Infants with weakened immune systems, particularly premature infants, are most likely to contract an Cronobacter infection, although the bacteria have caused illnesses in all

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

The FDA, along with CDC and state