FDA Warns of Bacterial Contamination in Infant Formula

On June 5th, 2024, the U.S. Food and Drug Administration (FDA) announced that Dairy Manufacturers Inc. is recalling their Crecelac Infant 0-12 month iron-fortified goat milk formula due to non-compliance with FDA infant formula regulations.

As part of an ongoing investigation, the FDA detected the presence of Cronobacter bacteria in a sample of the affected formula. Cronobacter bacteria can cause serious infections of the central nervous system and bloodstream, potentially leading to life-threatening conditions like sepsis and meningitis.

The recalled Crecelac formula has the UPC code 8 50042 40847 6 and a lot code of 24 039 1 CHE 352-1. It was sold primarily in Texas retail stores during March, April, and May of 2024. The product weight is 12.4 oz and has a best-by date of August 2025.

Fortunately, no illnesses have been reported in connection with this recall so far. The FDA is advising consumers to stop using the recalled product immediately and return it to the place of purchase for a full refund. Parents or caregivers who have used the affected formula and are concerned about their child's health should contact their healthcare provider.

This is the latest in a string of recent infant formula recalls in the U.S. due to non-compliance with federal safety standards. The FDA continues to closely monitor the industry to ensure the safety and quality of these critical products for the most vulnerable consumers.