Food Recall Check
Class I · High risk Terminated Initiated Nov 29, 2024 (2 years ago)

Cucumbers Slices 1/2 Cup recall

Recalled by Indianapolis Fruit Company, Inc. · Indianapolis, IN, United States

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

Why it was recalled

potential for salmonella

Pathogen: Salmonella

Salmonella is the most common cause of food recalls for bacteria, often in eggs, produce, nuts and spices.

The most serious food recalls: a contaminated product can cause outbreaks, hospitalisations and deaths, especially for pregnant people, young children, older adults and anyone with a weakened immune system. All bacteria & viruses recalls.

What was recalled

Cucumbers Slices 1/2 Cup, 100 cups per case, Product Code CUCS100, Item Number - 14705 Cucumbers Diced 1" Peeled 5 lb. tray, 2 trays per case, Product Code CUDN45L, Item Number - 9975 Cucumbers Slices 2 oz., 100 per case, Product Code CUS100, Item Number - 9816 Cucumbers Slices 2 oz. bag, 50 bags per case, Product Code CUS502, Item Number - 25473 Cucumbers Sliced 1/4" 5 lb. tray, Product Code CUS5L, Item Number - 2669

Quantity: 288 cases

Food: Cucumbers

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.

2531104

Where it was sold

Indiana Kentucky Ohio Pennsylvania

FDA's distribution note: IN, KY, OH, PA

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. 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
Indianapolis Fruit Company, Inc.
Initiated by
Voluntary: Firm initiated
Recall initiated
Nov 29, 2024
In FDA report of
Dec 25, 2024
Terminated
Mar 21, 2025
FDA recall number
F-0374-2025 · event 95932
Official record
FDA enforcement report search

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