Walmart, Broccoli and FDA

Broccoli recall: FDA upgrades recall to ‘deadliest level’ for florets sold at Walmart in 20 states, throw out ASAP
The recall announced in January involves contaminated broccoli sold in 20 states. Here's everything you need to know
FDA labels broccoli sold at Walmart as deadly. See where it was sold and what you should do
The U.S. Food and Drug Administration has labeled the broccoli recall as a Class I, the highest risk level issued by the agency.
Walmart broccoli recall: Was tainted food sold in Mississippi? FDA labels veggies deadly
Broccoli sold at Walmart in 20 states has been labeled potentially deadly in an update from the FDA. Was it sold in Mississippi? Here's what we know.
FDA upgrades recalled broccoli to highest level over possible Listeria contamination
The U.S. Food and Drug Administration upgraded the classification of recalled broccoli sold at Walmart originally issued in December to its highest recall category, according to the agency’s updated report.
Broccoli recall hits ‘deadly’ level: Here’s what to know.
The recall level has been elevated to the highest the U.S. Food & Drug Administration (FDA) has, meaning the broccoli may potentially be deadly to susceptible individuals. According to an FDA press release,
FDA warns of deadly risk in Walmart frozen broccoli
Nationwide health alert over listeria risk leads to major Walmart broccoli recall affecting 35,508 bags across 20 states as FDA warns of potential deadly consequences.
FDA Changes Raise Concerns About Food Recalls
The number of hospitalizations and deaths from foodborne illness doubled last year compared to 2023 in the U.S.
Time on MSN3d
FDA Approves the First Non-Opioid Pain Drug in 20 Years
The prescription pills, sold under the brand name Journavx and made by Vertex Pharmaceuticals, are taken twice a day and ...
FDA approves first new non-opioid painkiller in decades, and it's from a MA company.
The U.S. Food and Drug Administration approved a new non-opioid pain medication developed by the Massachusetts-based company ...
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FDA grants orphan drug status to Arbor Biotechnologies’ PH1
The US Food and Drug Administration (FDA) has granted orphan drug designation (ODD) and rare paediatric disease designation (RPDD) to Arbor Biotechnologies' gene editing therapeutic, ABO-101, to treat ...
Smithsonian Magazine9h
FDA Approves Transplant Trials for Gene-Edited Pig Kidneys
The FDA will allow two biotechnology companies to run clinical trials: United Therapeutics and eGenesis. United Therapeutics ...
The Washington Post10d
Americans might finally have to face what’s in their food
(Scott Olson/Getty Images) In the final days of the Biden administration, the Food and Drug Administration proposed ... including the FDA and the Centers for Disease Control and Prevention ...
MedCity News21h
“Precision Med Has Evolved as Badly As I Expected” And Other Takeaways From Former FDA Commissioner At PMWC
Robert Califf addressed a range of issues, including AI, lack of nutrition resources at the FDA and how he evaluates the progress of precision medicine at the Precision Medicine World Conference in ...
Dog food recalled over salmonella risk: Here’s what the FDA wants you to know
Blue Ridge Beef is recalling 5,700 pounds of its 2-pound log Natural Mix, according to the FDA, which warned that salmonella can affect animals, and there is risk to humans from handling the food, ...
Mini pastries contaminated with Salmonella sold in Florida, other states: FDA
Multiple people have fallen ill after consuming mini pastries contaminated with Salmonella, according to the U.S. Food and ...
U.S. FDA approves Supernus' drug-device combination for Parkinson's disease
The U.S. Food and Drug Administration has approved Supernus Pharmaceuticals' drug-device combination to treat ...