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House and Senate Oversight on Cronobacter and Infant Formula this week

Bill Marler

Now the House and Senate are set to ask questions of the Industry and FDA about how the outbreak happened and how it impacted the supply of infant formula. Here is a preview of the FDA’s position See full testimony – FDA Testimony ECOI Infant Formula 5.25.2022 final : TESTIMONY OF. CALIFF, M.D. COMMISSIONER OF FOOD AND DRUGS.

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DeLauro Shares Whistleblower Report, Contaminated Infant Formula Led to Hospitalizations and Deaths

Bill Marler

House Appropriations Committee Chair Rosa DeLauro (D-CT-03) today submitted for the record a report acquired from a whistleblower who worked at the Abbott facility which produces infant formula recalled by the United States Food and Drug Administration (FDA) in February. Below are Chair DeLauro’s remarks.

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FDA Relaxes Nutrition Facts and Menu Labeling Requirements for Restaurants and Food Manufacturers During COVID-19 Emergency

Modern Restaurant Management

Food and Drug Administration (FDA) has issued two temporary food labeling guidance documents that attempt to balance industry supply and demand during the novel coronavirus pandemic. The requirements apply to products, including ingredients, that are typically purchased by restaurants to further prepare for sale to consumers.

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FDA issues warning about LittleOak infant formula

Food Safety News

The FDA is alerting parents and caregivers about two varieties of LittleOak infant formulas that the company is currently recalling. Parents and caregivers of infants who have purchased these products should understand that they have not been evaluated to determine whether they meet U.S. food safety and nutritional standards.

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FDA sends warning letters to infant formula manufacturers, unveils Cronobacter history in facilities

Food Safety News

Mead Johnson Nutrition (Reckitt), and Perrigo Wisconsin, LLC. According to the FDA, this action is occurring within the context of its ongoing commitment to enhance regulatory oversight and reflects the agency’s determination to ensure optimal conditions for producing infant formula. 30, 2023, warning letter, the FDA described a Dec.

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FDA issues warning about certain supplements with toxic yellow oleander

Food Safety News

The Food and Drug Administration (FDA) has issued a warning about certain tejocote root supplements substituted with toxic yellow oleander. The FDA’s warning has prompted World Green Nutrition, Inc. Tejocotex Amazon.com Alipotec South TX World Green Nutrition, Inc. Additional sample analysis is pending.

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Jim Jones to Serve as First FDA Deputy Commissioner for Human Foods

Food Safety Tech

food supply in the face of climate change and globalization, as well as nutrition to help reduce diet-related diseases and improve health equity. Jones is scheduled to begin at the FDA on September 24, 2023. I’m delighted to welcome Jim to the FDA. For more than 30 years, Jones has held various positions in the U.S. Califf, M.D.

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