FDA Warns Parents Against Contaminated Texas Infant Formula

US health authorities advise parents to avoid Crecelac Infant Powdered Goat Milk Infant Formula from Texas-based Dairy Manufacturers Inc. after dangerous bacteria, cronobacter, was found in samples. The bacteria, which caused infant formula recalls in 2022, can lead to deadly infections in babies. The Farmalac brand from the same company was also recalled.


PTI | Washington DC | Updated: 01-06-2024 03:32 IST | Created: 01-06-2024 03:32 IST
FDA Warns Parents Against Contaminated Texas Infant Formula
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US health officials warned parents to avoid powdered infant formula sold by a Texas dairy producer, because a dangerous bacteria was found in one of the company's products.

The Food and Drug Administration issued the alert Friday on Crecelac Infant Powdered Goat Milk Infant Formula, after a sample collected from a Texas store tested positive for cronobacter, which can cause deadly infections in babies. The same bacteria sparked recalls and shortages of infant formula in 2022 after it was detected at a major US formula factory.

The Crecelac formula was imported and distributed by Dairy Manufacturers Inc., of Prosper, Texas, according to the FDA. Press releases from the FDA and the company did not specify where the product was produced or how widely it was distributed in the US Messages left for the company on Friday were not immediately returned.

Last week, the company voluntarily recalled the Crecelac formula and another brand, Farmalac, because they had not received approval by the FDA for sale in the US Infant formula distributors are required to submit data to FDA regulators showing their products meet US food and nutritional standards.

The FDA said testing of the Farmalac product did not detect cronobacter, but parents and caregivers should still avoid using the formula.

Cronobacter can cause blood infections and other serious complications in infants, including meningitis and nervous system injuries. The bacteria are found naturally in the environment and also can make their way into infant formula after packages are opened.

In 2022, FDA investigators shutdown an Abbott formula plant in Sturgis, Michigan, after inspections sparked by four infant illnesses linked to cronobacter, including two deaths, showed widespread contamination at the site.

Amid the shortages caused by the shutdown, the FDA began allowing imports of infant formula produced by overseas manufacturers. Previously the agency restricted US infant formula production to a handful of domestic manufacturers, including Abbott.

(This story has not been edited by Devdiscourse staff and is auto-generated from a syndicated feed.)

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