Food Recall Check
Class I · High risk Terminated Initiated Jan 19, 2025 (2 years ago)

FOOD SERVICE Mombo s Vanilla Soft Serve Ice Cream Mix recall

Recalled by Arizona Foods Group, Inc. · Phoenix, AZ, United States

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

Why it was recalled

Product may contain egg, an undeclared allergen.

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

FOOD SERVICE - Mombo s Vanilla Soft Serve Ice Cream Mix, frozen & thawed for Ice cream machines. Packaged in a half gallon carton 64 oz and placed in cases of 6-units. Shelf-life is 18 months frozen / 30 days thawed refrigerated. Carton is a plain white carton with a sticker label on one side and a code on the gable of the opposite side.

Quantity: 4,422 half gallon units, 737 cases

Food: Ice cream

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.

PLT 04-21 00925, Code is located on the gable of each half gallon unit

Where it was sold

Nevada

FDA's distribution note: Domestic distribution within NV.

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
Arizona Foods Group, Inc.
Initiated by
Voluntary: Firm initiated
Recall initiated
Jan 19, 2025
In FDA report of
Mar 5, 2025
Terminated
Mar 21, 2025
FDA recall number
F-0572-2025 · event 96165
Official record
FDA enforcement report search

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Reason Inaccurate Nutrition Facts information listed on product

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