The product, family-sized, 48-ounce cartons of Great Value Chicken Broth, are sold in aseptic paper cartons that could “compromise the sterility of the product, resulting in spoilage,” according to an announcement posted on the Food and Drug Administration’s website. Altogether, 2,023 cases have been recalled, according to the announcement.
According to the U.S. Food and Drug Administration ( FDA ), 2,023 cases of Great Value, Chicken Broth, sold in 48-ounce containers at Walmart, have been recalled. Each case includes six units of the product, meaning 12,138 cartons of broth were recalled.
A colorful ingredient you may find in your pantry or medicine cabinet is now banned by the Food and Drug Administration.
The recalled pancake and waffle mix was distributed in 11 states, including Kentucky and Indiana. The others are: Arkansas, Illinois, Iowa, Kansas, Minnesota, Mississippi, Nebraska, Utah and Wisconsin. There have been no reported allergic reactions to date.
Broth sold in Walmart stores has been assigned a risk class by the FDA after it was recalled over spoilage concerns.
As demand for weight-loss injections sold under brand names such as Ozempic and Wegovy continues to soar, a study has uncovered neurological and behavioral health benefits amid risks for pancreatitis and kidney disease.
Chicken broth sold by Walmart in several states, including Georgia, Oklahoma and Texas has been classified as a Class II recall. The broth was produced by Tree House Foods Inc., which is based in Canada, and was initially recalled on Dec. 11, 2024, according to the Food and Drug Administration notice.
Cattle farmers enjoyed record prices in 2024, but still had to contend with disease and rising input costs that cut into profit margins. The average for feeders more than
An Alabama woman is thriving a record 61 days and counting after receiving a pig kidney, a new milestone in the quest for animal-to-human transplants
Products were recalled because of concerns over salmonella and listeria contamination and undeclared allergens.
And the US Food and Drug Administration (FDA) has banned the use of red dye No. 3 in food, drinks, and ingested drugs. Laguarta said Pepsi doesn't have the dye in its US portfolio. The barrage of ...
Federal regulators have warned a Waco company that its human amniotic products are “unlicensed” and “unapproved,” and that its manufacturing process violates safety regulations. The U.S. Food & Drug Administration sent a warning letter to Frontier Biologics in November, outlining concerns about the company’s operations.