BORSARI Food Company Incorporated recall
Recalled by Borsari Food Company Inc · Jamestown, NY, United States
Class II — Moderate risk. May cause temporary or reversible harm; serious harm unlikely.
Why it was recalled
Product contains undeclared fish (anchovy) and soy.
Undeclared allergens: Soy Fish
For someone with a food allergy the label is the only protection. An undeclared allergen can trigger a severe reaction even in a trace amount, which is why most of these recalls are Class I. All undeclared allergens recalls.
What was recalled
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
Quantity: 5,818 units
Lot codes, dates and UPCs
A recall covers only these codes. Compare them with the lot number, best-by date or UPC printed on your package.
All products within expiry.
Where it was sold
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
FDA's distribution note: 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
Check the codes, then return or discard. Class II means eating it may cause temporary or reversible health problems. If your package matches the recalled codes, do not eat it - return it to the store or throw it away. The risk from an undeclared allergen is to people allergic to soy, fish; for anyone else the product is generally not a safety concern. FDA lists this recall as terminated: the company has finished removing the product, so it should no longer be on shelves - but it can still be in a freezer or pantry.
- Recalling firm
- Borsari Food Company Inc
- Initiated by
- Voluntary: Firm initiated
- Recall initiated
- Dec 9, 2024
- In FDA report of
- Jan 1, 2025
- Terminated
- Mar 14, 2025
- FDA recall number
- F-0317-2025 · event 95945
- Official record
- FDA enforcement report search