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FDA: Another infant death likely linked to Abbott formula

Bill Marler

The FDA apparently became aware of the death on June 10, 2020. So far, the FDA has received 129 complaints linked to Abbott formula products, including 119 since the product recall in February. According to the FDA, this would bring the total to five illnesses with three deaths. Attorney sued Abbott and several employees.

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Key Takeaways from the 2022 FDA Food Code

Modern Restaurant Management

In the waning days of 2022, FDA issued an updated Food Code with several important updates. FDA is responsible for more than a quarter of the U.S. Let’s examine the key new provisions of the 2022 Food Code. Many of the key changes in the 2022 Food Code relate to food allergens. goes uneaten.

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Citizen Journalism at its best – eFoodAlert and insights into “Abbott Nutrition: The Gathering Storm”

Bill Marler

Between September 1, 2019 and September 20, 2021, Abbott Nutrition received seventeen consumer complaints regarding multiple Similac powdered formula products. APPLIED – FOI II – BR Abbott Nutritions- FEI# 1815692 9-2021 EIR. The complaint was reviewed by an internal Abbott Nutrition Medical Team. FDA not blameless.

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FDA review panel picked to help fix FDA

Bill Marler

Dr. Jane Henney, former FDA Commissioner, was named as Chair of the panel last month. This team brings the right combination of FDA and other government experience along with deep subject matter expertise and first-hand systems and operations knowledge,” said Jane E. “We

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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. MAY 25, 2022. CALIFF, M.D. MAYNE, PH.D.

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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 to allow Abbott to release product to individuals needing urgent, life-sustaining supplies of the specialty and metabolic formulas – with a Warning

Bill Marler

How confident should we feel with this waring from the FDA: “those seeking access [to the formula] should consult with their healthcare provider in considering whether the benefit of consuming such product outweighs the potential risk of bacterial infection in the user’s particular circumstances.”.

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