Food Recall Check
Class I · High risk Terminated Initiated Nov 23, 2020 (6 years ago)

Prairie Farms 1% Lowfat Chocolate Milk recall

Recalled by Prairie Farms · Edwardsville, IL, United States

Class I — High risk. Reasonable probability of serious harm or death.

Why it was recalled

The product contains undeclared egg.

Undeclared allergen: Egg

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

Prairie Farms 1% Lowfat Chocolate Milk, 1 gallon, UPC 72730-26126

Quantity: 797 gallons

Food: Milk & dairy Chocolate & candy

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.

BEST BY DEC 04 2020

Where it was sold

Illinois Wisconsin

FDA's distribution note: retail outlets in the Chicago area, including the Northern Illinois Suburbs, Rockford, Illinois, and Southeastern Wisconsin

Do not eat it. Class I means FDA judged there is a reasonable probability of serious illness or death. If the brand, size and lot or date code on your package match, throw the product away or return it to the store for a refund, and clean any surface or container it touched. If anyone has eaten it and feels unwell, contact a doctor and mention the recall. The risk from an undeclared allergen is to people allergic to egg; 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
Prairie Farms
Initiated by
Voluntary: Firm initiated
Recall initiated
Nov 23, 2020
In FDA report of
Dec 16, 2020
Terminated
Dec 23, 2020
FDA recall number
F-0160-2021 · event 86852
Official record
FDA enforcement report search

Also recalled with it (1 more product)

FDA files each product of one recall action separately; these share the same FDA event.

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