recall fda - Search News

Order byBest matchMost fresh

FDA, frozen shrimp

The FDA’s radioactive shrimp recall now includes more brands: See the full list of impacted products

Southwind Foods has issued a voluntary recall of frozen shrimp products due to potential radioactive contamination, according to the company and an alert issued Thursday by the Food and Drug Administr...

· 1d · on MSN

FDA recalls more potentially radioactive frozen shrimp sold in the US

· 3d

Walmart recalls Great Value shrimp after FDA warns of risk of radioactive contamination

· 1d

Even More Shrimp Just Got Recalled Because of Radiation, at More Grocery Stores

"If you were eating shrimp all the time, like on a daily basis, then there might be more concern," Kowalcyk told the NYT.

· 1d

The Radioactive Shrimp Recall Gets Jumbo-Sized

MLive · 1d

Your frozen shrimp might be radioactive; FDA issues urgent recall across multiple states

2don MSN

Noodle recall update as FDA issues risk warning

The FDA classifies this recall as Class II, which the agency describes as a situation "in which use of or exposure to a violative product may cause temporary or medically reversible adverse health consequences or where the probability of serious adverse health consequences is remote."

Parade on MSN1d

FDA Issues Recall on Popular Soda That Could Pose Serious Health Risks—Here’s What You Need to Know

For those who do not need to watch sugar intake, the recall is mostly informational. The soda is safe to drink, but if you prefer the zero-sugar version you intended to buy, retur

Fierce Pharma3d

Alembic, Sun and Glenmark issue US drug recalls due to the presence of carcinogens or foreign matter

A trio of Indian drugmakers—Alembic Pharmaceuticals, Sun Pharmaceutical and Glenmark Pharmaceuticals—issued separate voluntary U.S. drug recalls in recent weeks due to either the presence of carcinogens or foreign matter in the products.

10don MSN

Nationwide Deodorant Recall Update as FDA Sets Risk Level

The recall of three Power Stick deodorants, affecting more than 67,000 products sold across the United States, was voluntary issued by Pennsylvania-based maker A.P. Deauville on July 10. FDA inspectors classified the recall a Class II on July 31.