Food FDA Class II Terminated Undeclared allergen
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, yel
Borsari Food Company Inc Published Jan 1, 2025
Risk level
Class IIMay cause a temporary or reversible health problem; slight chance of serious harm.
Severity score 62/100
What should you do?
- Check whether you have this product, using the lot codes, UPCs, and dates listed below.
- If you are allergic or sensitive to the ingredient noted, do not eat it — it could cause a serious reaction.
- Return it to the place of purchase for a refund, or throw it away in a sealed bag so people and animals can’t get to it.
- Contact Borsari Food Company Inc or your place of purchase with questions, and see the source record below for full details.
Reason for recall
Product contains undeclared fish (anchovy) and soy.
Hazards
Fish (Anchovy) · primarySoybeans
Affected products (1)
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
5,818 units
Code info: All products within expiry.
Affected areas
AlabamaArizonaCaliforniaConnecticutFloridaGeorgiaIllinoisIndianaKansasMarylandMassachusettsMichiganMinnesotaMontanaNew MexicoNew YorkOhioPennsylvaniaRhode IslandSouth CarolinaSouth DakotaTennesseeUtahVirginiaWashington
Timeline
- InitiatedDec 9, 2024
- PublishedJan 1, 2025
- TerminatedMar 14, 2025
- Recall number
- F-0317-2025
- Agency
- U.S. Food and Drug Administration
- Country
- US
FDA records come from the openFDA food enforcement-report dataset — the agency's full weekly enforcement list. Most entries are not issued as consumer press releases, so they won't appear on fda.gov/recalls or in a web search. The source record link above resolves this exact recall by its number.