Class IITerminatedVoluntary: Firm initiated
Borsari Food Company Inc: food recall F-0317-2025
Borsari Food Company Inc of Jamestown, NY recalled BORSARI Food Company Incorporated; BLOODY MARY MIX ; 32 FL. OZ; INGREDIENTS: Tomato juice, corn syrup, non-fat milk… Reason: Product contains undeclared fish (anchovy) and soy. The FDA listed it as Class II in its Enforcement Report dated Jan 1, 2025; distribution: 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, Washington.
Record status as published: Terminated (terminated Mar 14, 2025). openFDA data last updated Oct 21, 2026.
Have this product? Check FDA.gov and your retailer. This page reproduces an FDA Enforcement Report record and is not a public alert. Look for the firm's recall notice on the FDA's recalls page, or ask the store where you bought it what to do. If you think you got sick from a food, contact a health care provider.
Recall details
- Product
- BORSARI Food Company Incorporated; BLOODY MARY MIX ; 32 FL. OZ; INGREDIENTS: Tomato juice, corn syrup, non-fat milk solids, orange juice, lemon juice, lime juice, cayenne pepper, vinegar, salt, garlic powder, Worcestershire sauce, prepared horseradish, maltic acid, sodium and potassium benzoate, yellow 5 & 6; UPC: 815893000101
- Product quantity
- 5,818 units
- Reason for recall
- Product contains undeclared fish (anchovy) and soy.
- Codes, lots and dates on the package
- All products within expiry.
- Distribution pattern
- AL, AZ, CA, CT, FL, GA, IL, IN, KS, MA, MD, MI, MN, MT, NM, NY, OH, PA, RI, SC, SD, TN, UT, VA, WA
- Recalling firm
- Borsari Food Company Inc, Jamestown, NY
- Classification
- Class II — the FDA uses this class for a situation in which using or being exposed to the product may cause temporary or medically reversible adverse health consequences, or where the probability of serious adverse health consequences is remote.
- Voluntary or mandated
- Voluntary: Firm initiated
- How the firm first notified customers
- Press Release
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Dates
| Event | Date |
|---|---|
| Recall initiated by the firm | Dec 9, 2024 |
| Classified by the FDA | Dec 24, 2024 |
| Published in the Enforcement Report | Jan 1, 2025 |
| Terminated | Mar 14, 2025 |
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Sources
- U.S. Food and Drug Administration, openFDA food enforcement reports, recall number F-0317-2025 (openFDA record). Data provided by the U.S. Food and Drug Administration (https://open.fda.gov).
- Do not rely on openFDA to make decisions regarding medical care. While we make every effort to ensure that data is accurate, you should assume all results are unvalidated. We may limit or otherwise restrict your access to the API in line with our Terms of Service. The FDA does not endorse OpenPlate.