Lower riskFood recall · FDA · Published December 24, 2020
Lipari Backroad Country Spicy Cajun Mix: Undeclared Milk Allergen Hazard
Lipari Foods recalls Backroad Country Spicy Cajun Mix (9oz) due to undeclared milk allergen. Consumers should check lot numbers M24501, M26902, M28201 for affected products.
“Lipari Backroad Country Spicy Cajun Mix: Undeclared Milk Allergen Hazard.” GovInfoNow, updated October 4, 2026. https://govinfonow.com/recall/14966-lipari-backroad-country-spicy-cajun-mix-undeclared-milk-allergen-hazard. Based on FDA recall #F-0199-2021 (https://api.fda.gov/food/enforcement.json?search=recall_number:%22F-0199-2021%22&limit=1).
The FDA announced on Dec. 24, 2020, that Lipari Foods Operating Company, LLC. voluntarily recalled Backroad Country Spicy Cajun Mix due to undeclared milk allergens. The agency issued recall number F-0199-2021 for the Class I food product.
How to tell if you have it
Brand: Lipari Foods
Product: Backroad Country Spicy Cajun Mix 9 oz (255g) plastic bag
The product contains undeclared milk allergens. The FDA classified this as a Class I recall, indicating a reasonable probability that the food will cause serious adverse health consequences or death.
Context
GovInfoNow's records show Lipari Foods Operating Company, LLC. has 11 other recalls on record since 2018-12-11. Recent brand recalls include a June 18, 2025 undeclared milk hazard for Dark Chocolate Nonpareils and a June 27, 2024 salmonella risk for Premo Turkey & Swiss. Other recent recalls of similar products include B.C. Williams Bakery Spice Cake Mix (Dec. 23, 2025), Wawa Diet Lemonade P (April 2, 2026), and Savor Seasonings Organic Cheddar Seasoning (Aug. 7, 2026).
How to tell if you have this one
Check the product for lot numbers M24501, M26902, or M28201. The product is a 9oz plastic bag labeled as Backroad Country Spicy Cajun Mix.
Brand
Lipari Foods
Category
Food
Based on the official FDA remedy
What to do — step by step
Check Product Lot Numbers
Look for lot numbers M24501, M26902, or M28201 on the packaging.
Where it went and when
Where it was distributed
Distributed in 20 states.
Listed by the agency
Not listed
FDA distribution: “Product was distributed to the following states: Alabama Arkansas Colorado Georgia Illinois Indiana Kansas Maryland Michigan Missouri Mississippi Nebraska Ohio Oklahoma Pennsylvania South Carolina Tennessee Texas Virginia Wisconsin” States read from FDA’s own wording; “not listed” means the notice does not name it.
The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
Official source: FDA Recall #F-0199-2021 (December 24, 2020) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for F-0199-2021 to see it in context.
Plain-language summary written by qwen3:4b on October 4, 2026, from the official record above. Not reviewed by a person — if it conflicts with the FDA notice, the notice is correct. Report an error on this page.
GovInfoNow is an independent service and is not a government agency. We republish official FDA recall data; we don’t issue, amend or administer recalls.