Food Recall Check
Class I · High risk Terminated Initiated Jul 8, 2025 (15 months ago)

Sheehan Brothers Vending Cheeseburger recall

Recalled by Sheehan Brothers Vending · Springfield, OH, United States

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

Why it was recalled

Undeclared sesame

Undeclared allergen: Sesame

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

Sheehan Brothers Vending Cheeseburger, 4.7 oz (132g), individually wrapped in plastic, UPC: 100000952375

Quantity: 824 individual units

Food: Cheese

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.

Prepared: Jul 1, 2025 and Sell By: Jul 7, 2025 Prepared: Jul 6, 2025 and Sell By: Jul 12, 2025

Where it was sold

Indiana Kentucky Ohio

FDA's distribution note: IN, KY, OH

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 sesame; 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
Sheehan Brothers Vending
Initiated by
Voluntary: Firm initiated
Recall initiated
Jul 8, 2025
In FDA report of
Aug 6, 2025
Terminated
Sep 17, 2025
FDA recall number
H-0331-2025 · event 97225
Official record
FDA enforcement report search

Also recalled with it (5 more products)

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

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