A small batch of Frito-Lay chips was recalled in late March over an undeclared allergen.. The American food company issued a voluntary recall last month for about 1,300 bags of Tostitos Cantina ...

Frito-Lay is reading the writing on the wall and making changes to some of its most popular snacks, in an effort to cater to ...

Anyone with questions can call Frito-Lay's customer support line at 800-352-4477 during office hours Monday between 10 a.m. and 5:30 p.m. EST. Brand recalled over 6,000 classic potato chips last year ...

The Food and Drug Administration increased the recall of one of Frito-Lay's most popular chips, noting they "could cause death," WKRC reported. Tostitos Cantina-style corn chips were first ...

People would have been able to buy the recalled chips as early as March 7, 2025, according to the company. Frito-Lay told USA TODAY on March 26 that the voluntary recall does not impact any other ...

This is not the first time the company has recalled a product for this particular matter. In December, Frito-Lay issued a recall for over 6,000 bags of 13 oz. bags of Lay’s Classic Potato Chips ...

Frito-Lay is voluntarily recalling a limited number of Tostitos tortilla chips that could contain an undeclared milk allergen, the company announced. The recall affects fewer than 1,300 bags of 13 ...

Anyone with questions can call Frito-Lay's customer support line at 800-352-4477 during office hours Monday through Friday between 10 a.m. and 5:30 p.m. ET. Frito-Lay recalled over 6,000 classic ...

Frito-lay is recalling a brand of tortilla chips sold in 13 states. Here's why. Skip to Article. Set weather. ... According to Frito-Lay, less than 1,300 chip bags were affected.

Frito-Lay is recalling a limited number of Tostitos tortilla chips because they may contain undeclared milk. The company said Wednesday that the recall includes less than 1,300 13-ounce bags of ...

On Dec. 13, Frito-Lay voluntarily recalled more than 6,000 bags of 13 oz. Lay’s Classic Potato Chips due to undeclared milk. But, by Jan. 27, the FDA classified the issue as a Class 1 recall.