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You are at:Home » FDA upgrades cookie recall to highest danger level over undeclared peanuts
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FDA upgrades cookie recall to highest danger level over undeclared peanuts

Press RoomBy Press RoomJanuary 23, 2026No Comments2 Mins Read
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FDA upgrades cookie recall to highest danger level over undeclared peanuts
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The Food and Drug Administration announced that a recall of cookie products has been upgraded to its most serious risk category over the potential presence of undeclared peanuts.

Gregory’s Foods first issued a recall last month of its 2-pound 8.5-ounce packages of “Bag Full of Cookies” White Chocolate Macadamia Nut frozen cookie dough after learning that some packages were mistakenly filled with Monster Cookie Dough, which contains peanuts.

“People who have allergies to peanuts run the risk of serious or life-threatening allergic reaction if they consume these products,” the FDA said in its announcement at the time.

RECALL OF CHEESE PRODUCTS UPGRADED TO HIGHEST DANGER LEVEL OVER LISTERIA-CAUSING BACTERIA: FDA

The FDA then announced on Wednesday that the recall has been reclassified as Class I, its highest level of concern. A Class I recall means there is a “reasonable probability that the use of, or exposure to, [the] product will cause serious adverse health consequences or death.”

The recall affects more than 300 cases, with six bags in each case. The impacted products have a best by date of Dec. 6, 2026.

The U.S. Food and Drug Administration headquarters

“Observable through the clear window in the bag, the Monster Cookies frozen dough has visible chocolate chips and colored candy-coated pieces whereas the White Chocolate Macadamia Nut frozen cookie dough does not,” the FDA said in December.

The cookie products were sold in retail grocery stores in Minnesota, Nebraska, North Dakota and Wisconsin.

TRIO OF DAIRY GIANTS RECALL INFANT FORMULA OVER CONTAMINATION FEARS

FDA headquarter sign

Customers are urged not to consume the product and to return the product to the place of purchase for a full refund.

The FDA said the issue was isolated to certain units in one day’s production and has been corrected.

Read the full article here

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