Food Recall Check
Class II · Moderate risk Terminated Initiated Mar 25, 2025 (2 years ago)

Lillie's Q Buffalo Wing Sauce recall

Recalled by Old World Spices & Seasoning, INC · Overland Park, KS, United States

Class II — Moderate risk. May cause temporary or reversible harm; serious harm unlikely.

Why it was recalled

Undeclared allergen (milk not listed as sub ingredient of butter). Milk also not listed in 'Contains' statement.

Undeclared allergen: Milk

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

Lillie's Q Buffalo Wing Sauce. Net wt. 13.5 oz, UPC 810069510972, Case label: Lillie's Q Buffalo Wing Sauce, Item # FGLOL422 Lot # 002125, 6/13.5 oz, UPC 10810069510979, BEST BY: JAN/21/2026

Quantity: 8,532 bottles

Food: Sauces, dips & dressings

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.

Lot #002125, BEST BY: JAN/21/2026 Lot #002025; BEST BY: JAN/20/2026 Lot #005725; BEST BY: FEB/25/2026

Where it was sold

California Colorado Connecticut Florida Georgia Iowa Kansas New Hampshire New York Pennsylvania Texas Washington Wisconsin

FDA's distribution note: Distribution Centers located in: KS, FL, NH, CA, IA, GA, TX, CO, CT, WI, NY, WA, PA

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 milk; 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
Old World Spices & Seasoning, INC
Initiated by
Voluntary: Firm initiated
Recall initiated
Mar 25, 2025
In FDA report of
Apr 16, 2025
Terminated
Sep 24, 2025
FDA recall number
F-0699-2025 · event 96602
Official record
FDA enforcement report search

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