The U.S. Food and Drug Administration (FDA) has categorized the recall of Borsari Food Company Inc.’s Bloody Mary Mix as a Class II risk following an announcement made on December 24, 2025.
The recall, initiated earlier this month, includes 5,818 units of the 32 oz. Bloody Mary Mix bottles distributed across 25 states: Alabama, Arizona, California, Connecticut, Florida, Georgia, Illinois, Indiana, Kansas, Massachusetts, Maryland, Michigan, Minnesota, Montana, New Mexico, New York, Ohio, Pennsylvania, Rhode Island, South Carolina, South Dakota, Tennessee, Utah, Virginia, and Washington.
The product, containing a mix of tomato juice, corn syrup, non-fat milk solids, various fruit juices, spices, and preservatives, was recalled due to undeclared allergens – fish (anchovy) and soy.
No illnesses have been reported, but the presence of these allergens poses a risk of severe allergic reactions to sensitive individuals.
The FDA defines a Class II recall as one where “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.”
This classification suggests a medium to low risk level for consumers, although caution is still advised.
Borsari Food Company has committed to updating their labels to clearly declare all ingredients, including fish (anchovy) and soy, on both current in-house inventory and future products.
The recalled product comes in a clear 32 oz. plastic bottle with a black label prominently displaying the Borsari brand and the words “Bloody Mary Mix” in large block letters.
The UPC code for this product is 815893000101.
Consumers who have purchased this product are encouraged to return it. Borsari is actively contacting customers to offer replacements upon proof of purchase.
For further inquiries, customers can contact Borsari Food Company at 716-763-3391.