food and drug administration

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FDA recalls shrimp sold at Walmart

Shrimp, salad kits and more: See list of FDA food recalls in 2025 so far

Fresh & Ready Foods, LLC, recalled a few of their ready-to-eat products, including sandwiches and other snack items, over fears of Listeria contamination in May this year. According to the Centers for Disease Control and Prevention (CDC), one person died and 10 people required hospitalization due to Listeria contamination in two states.

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FDA urges recall of Walmart shrimp over radioactive contamination fear

· 18h

Walmart Recalls Frozen Shrimp Over FDA Warning About Radiation Risk

· 13h

The FDA Issues Warning for Potentially Radioactive Shrimp Sold at Walmart

On August 19, the United States Food & Drug Administration (FDA) unlocked a new fear for shrimp lovers everywhere.

· 20h

Walmart recalls possibly radioactive shrimp after public warned not to eat

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FDA Warns Potentially Radioactive Shrimp Sold at Walmart in 13 States

· 13h

Walmart recalls frozen shrimp in 13 U.S. states over risk of radioactivity

The risk from the recalled shrimp is "quite low," said Donald Schaffner, a food safety expert at Rutgers University.

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Walmart shrimp may have been exposed to radioactive material, FDA says

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Don't eat these potentially radioactive shrimp, FDA warns

22hon MSN

FDA approves use of animal drugs to treat New World Screwworm

The Food and Drug Administration has authorized emergency use of animal drugs to treat and prevent infestations of the New World Screwworm, which poses an emerging threat to U.S. livestock and food security.

4hon MSN

Orland Park family fights FDA over approval of drug to treat rare genetic disease

A little boy in the Chicago area is battling a rare disease and desperately needs a drug treatment for a better life. The drug has not been FDA approved, and it could disappear if it isn't soon.

The Well News on MSN15h

FDA Cleared to Use Animal Drugs to Combat New World Screwworm Threat

WASHINGTON - The Food and Drug Administration was authorized Tuesday to use "animal drugs" on an emergency basis to treat and prevent infestations of the New World screwworm, a flesh-eating parasite that poses a threat to the U.

1don MSN

US FDA declines to approve PTC Therapeutics' oral drug for rare genetic disorder

The U.S. Food and Drug Administration has denied approval for PTC Therapeutics' oral medication for a rare genetic disorder with limited treatment options, the company said on Tuesday.

2don MSN

FDA’s new expert panels are rife with financial conflicts and fringe views

A series of panels convened by the Food and Drug Administration is raising concerns that the agency is skirting federal rules and promoting fringe views about antidepressants and other products.

1don MSN

HHS will allow emergency use of animal drugs in New World screwworm fight

The Food and Drug Administration (FDA) became authorized Tuesday to allow the use of animal drugs to treat or prevent infestations caused by the New World screwworm, a flesh-eating parasite that has recently disrupted the cattle industry.

Over 5,000 lbs. of cheese recalled by FDA due to contamination concerns over 'serious and sometimes fatal' bacteria

More than 5,000 pounds of cheese products made by Middlefield Original Cheese Co‑op are being voluntarily recalled after the company discovered contamination by potentially deadly bacteria, according to the Food and Drug Administration.

14h

America’s fragile drug supply chain is extremely vulnerable to climate change

More than 60 percent of US drug facilities are in areas with weather disasters.

USA Today1y

From vaping to abortion, conservatives are targeting FDA authority

The 5th Circuit ruled on Aug. 16 that it would limit access to mifepristone, finding that the Food and Drug Administration overstepped its authority with a series of actions that made it easier ...

Stealth resubmits rare disease drug to FDA

The biotech, which cut jobs following the rejection in May of its Barth syndrome therapy, claimed it has addressed the agency’s concerns and now sees potential for a speedy review.

Pharmaceutical Technology on MSN20h

FDA awards breakthrough therapy status to BMS and SystImmune’s NSCLC drug

Bristol Myers Squibb and SystImmune have announced breakthrough therapy designation from the US Food and Drug Administration (FDA) for izalontamab brengitecan (iza-bren) to treat locally advanced or metastatic non-small cell lung cancer (NSCLC) with specific epidermal growth factor receptor mutations.