Lower riskFood recall · FDA · Published November 23, 2020
Prairie Farms Chocolate Milk Recall: Undeclared Egg in Product
Prairie Farms recalls 1-gallon chocolate milk with undeclared egg. Consumers should check UPC 72730-26110 and avoid use due to potential allergen risk.
“Prairie Farms Chocolate Milk Recall: Undeclared Egg in Product.” GovInfoNow, updated October 4, 2026. https://govinfonow.com/recall/15005-prairie-farms-chocolate-milk-recall-undeclared-egg-in-product. Based on FDA recall #F-0161-2021 (https://api.fda.gov/food/enforcement.json?search=recall_number:%22F-0161-2021%22&limit=1).
Prairie Farms recalled 355 gallons of Premium Flavored Chocolate Milk due to undeclared egg, according to the FDA on Nov. 23, 2020. The Class I recall affects product with UPC 72730-26110 sold in the Chicago area and Southeastern Wisconsin.
The product contains undeclared egg, posing an allergy risk to consumers. The FDA classified the recall as Class I.
Context
GovInfoNow's records show other recent recalls of similar products include B.C. Williams Swiss Chocolate Cake Mix (2025-12-23), The Better Bakehouse Donutful Donuts (2026-08-17), and Winfield's CWB Chocolate Bar (2026-04-27).
How to tell if you have this one
Check for the UPC 72730-26110 on the product label. The product was sold with a best-by date of December 4, 2020.
FDA lists each product line separately under one recall event. Check your product description, lot or code numbers against each row. Every row shares the hazard and remedy on this page.
Classification
Class I
Status
Terminated
Distribution
retail outlets in the Chicago area, including the Northern Illinois Suburbs, Rockford, Illinois, and Southeastern Wisconsin
Recall number
Product, codes & lots
Quantity
F-0160-2021
Prairie Farms 1% Lowfat Chocolate Milk, 1 gallon, UPC 72730-26126; BEST BY DEC 04 2020
797 gallons
F-0161-2021
Prairie Farms Premium Flavored Chocolate Milk, 1 gallon, UPC 72730-26110; BEST BY DEC 04 2020
355 gallons
Based on the official FDA remedy
What to do — step by step
Check Product Label
Look for the UPC 72730-26110 on the product label to confirm if it is recalled.
Where it went and when
Where it was distributed
Distributed in Illinois and Wisconsin.
Listed by the agency
Not listed
FDA distribution: “retail outlets in the Chicago area, including the Northern Illinois Suburbs, Rockford, Illinois, and Southeastern Wisconsin” States read from FDA’s own wording; “not listed” means the notice does not name it.
States: Illinois, Wisconsin.
Recall timeline
FDA terminated this recall 30 days after the firm started it.
1Firm started the recall
2FDA classified it Class I
3Published in FDA’s Enforcement Report
4FDA terminated the recall
Dates from the agency record only; steps without a date are left out.
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-0161-2021 (November 23, 2020) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for F-0161-2021 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.