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Reckitt/Mead Johnson Nutrition received a warning for significant violations of infant formula Current Good Manufacturing Practice (CGMP) requirements at two powdered infant formula facilities in Zeeland, Michigan and Wanamingo, Minnesota. FDA inspections conducted between November 2022 and February 2023 identified violations of Title 21 CFR Part 106, which governs infant formula manufacturing, quality control procedures, quality factors, records and reports, and notifications. The company's violations of the Federal Food, Drug, and Cosmetic Act rendered its infant formula products adulterated, representing a critical safety and compliance failure in a category of products subject to heightened regulatory scrutiny.