Infant Formula (Crecelac) – notification issue (2024)
Class I: A situation in which there is a reasonable probability that the use of, or exposure to, a violative product will cause serious adverse health consequences or death
Class I recall indicates potential for serious health consequences.
This AI-generated summary is provided for general informational purposes only and is derived from publicly available recall notices. It supplements but does not replace official agency classifications or safety instructions.
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
Crecelac Infant 0-12 powdered infant formula with iron 12.4 oz cans
Brand
Dairy Manufacturers, Inc
Lot Codes / Batch Numbers
24 039 1 CHE 352-1 02/09/2024 AUG/2025 24 062 1 CHE 352-1 03/08/2024 SEP/2025
Products Sold
24 039 1 CHE 352-1 02/09/2024 AUG/2025 24 062 1 CHE 352-1 03/08/2024 SEP/2025
Dairy Manufacturers, Inc is recalling Crecelac Infant 0-12 powdered infant formula with iron 12.4 oz cans due to The firm has not submitted the required premarket notification, parents and caregivers should understand that the products have not been evaluated to . This is a Class I recall, indicating a high risk of serious health consequences. Based on FDA enforcement report.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
The firm has not submitted the required premarket notification, parents and caregivers should understand that the products have not been evaluated to determine whether they meet U.S. food safety and nutritional standards. Cronobacter spp. detected by FDA sampling.
Recommended Action
Per FDA guidance
Consumers should stop using the product and contact the recalling firm or return it to the place of purchase.
Verify this information on the official source
For complete details and official instructions, check the U.S. Food and Drug Administration (FDA) directly.
View official FDA recall noticeDistribution
As reported by FDA
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Page updated: Jan 6, 2026