Two babies in US infected with rare bacteria found in infant formula
Dangerous bacteria that sparked powdered formula recalls and shortages last year has infected two babies this year, says US govt body
The dangerous bacteria that sparked powdered formula recalls and shortages last year has infected two babies this year, killing a Kentucky child and causing brain damage in a Missouri infant.
Federal health officials confirmed Thursday that two cases of invasive infections caused by cronobacter sakazakii have been reported in 2023, both in infants who consumed powdered infant formula made by Abbott Nutrition, the company at the centre of the 2022 crisis.
Food and Drug Administration officials said there was no evidence that the infections were linked to manufacturing and no reason to issue new recalls. The bacteria are found naturally in the environment and also can make their way into infant formula after the packaging is opened.
“There is no indication of a broader public health concern related to this product at this time,” the FDA said in a statement.
Kentucky health officials notified the Centres for Disease Control and Prevention on Nov 15 that a child who consumed Similac Total Care powdered formula died after being infected with cronobacter sakazakii.
In Missouri, 6-week-old Mira White, of Sikeston, was diagnosed in early March with a brain infection caused by the bacteria, which was detected in an open container of Similac NeoSure formula in her home.
The same type of bacteria led federal investigators to shut down an Abbott formula plant in Sturgis, Michigan, last year when inspections sparked by four infant illnesses, including two deaths, showed widespread contamination in the plant.
Since falling ill, Mira has suffered nearly constant seizures and inconsolable bouts of crying, said her 33-year-old mother, Asian Davis. Brain scans showed neurological damage and missing tissue caused by the infection.
“It affected her brain real bad,” Davis said. “She'll grow, but it will be a slow progress.” FDA investigators said they “did not identify a causal link” between Mira's infection and the Casa Grande, Arizona, factory that made the formula marketed for premature babies. Abbott officials said they found no cronobacter in batches of formula at the plant. The bacteria also weren't found in unopened cans of Similac NeoSure formula from Mira's home.
In Kentucky, the FDA said it “has not found evidence” of contamination after a Nov 21 inspection at an Abbott plant. Officials did not identify the child or the location of the plant.
Abbott officials said there is no evidence that conditions at the company's manufacturing plants or contamination in sealed products caused the illnesses.
Frank Yiannas, a former FDA official in charge of food safety response, cautioned that a negative test does not guarantee there's no contamination.
“A positive test result means a lot. A negative test result doesn't mean anything," he said.
Food safety advocates say the tragic cases underscore the overlooked risk of powdered formula, particularly for babies born prematurely, as Mira was. And it highlights the need for better education for parents and caregivers about how to prepare and use the crucial food.
Many people don't understand that powdered infant formula isn't sterile, said Mitzi Baum, chief executive of the nonprofit group STOP Foodborne Illness.
The powder itself can harbour potentially dangerous germs — and it is easily contaminated by sources in the home. Cronobacter sakazakii bacteria are common in soil and surface water, as well as dry foods.
Very young babies and those born prematurely are vulnerable to illnesses caused by the germ because their immune systems aren't developed enough to fight it off.
(Except for the headline, this story has not been edited by The Federal staff and is auto-published from a syndicated feed.)