RecallHawk
Class I Recall

Cucumbers Slices 1/2 Cup, 100 cups per case, Product Code CUCS100, Item Number - 14705 Cucumbers Diced 1" Peeled 5 lb.

Indianapolis Fruit Company, Inc.

Summary

The FDA issued a Class I for Cucumbers Slices 1/2 Cup, 100 cups per case, Product Code CUCS100, Item Number - by Indianapolis Fruit Company, Inc.. Reason: potential for salmonella.

Details

Source

Food Recall

External ID

F-0374-2025

Action Date

2024-12-25

Status

Terminated

Category

food

Product Description

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

Lot/Code Info: 2531104

Quantity Affected: 288 cases

Reason for Recall

potential for salmonella

Distribution

IN, KY, OH, PA

Type: Voluntary: Firm initiated

Recall Initiated: 2024-11-29

Company

Context & Analysis

This is a Class I recall. Class I recalls are the most serious — there is a reasonable probability that use of or exposure to the product will cause serious health consequences or death.

This was one of 53 food recalls issued in the same week, part of 204 food-related FDA actions this month.

Indianapolis Fruit Company, Inc. has 4 FDA actions in our database, including 4 recalls.

Frequently Asked Questions

What is a Class I recall?

A Class I recall is the most serious type. The FDA has determined there is a reasonable probability that the product will cause serious adverse health consequences or death. Consumers should stop using the product immediately.

What should I do if I have this product?

Stop using the product. Check the product against the specific lot numbers or identifiers listed in the recall. Contact the manufacturer (Indianapolis Fruit Company, Inc.) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.

How often does Indianapolis Fruit Company, Inc. have FDA actions?

Indianapolis Fruit Company, Inc. has 4 FDA actions in our database, including 4 recalls and 0 device clearances.

Where can I find the official FDA record?

The official record is available on FDA.gov. Search for "F-0374-2025" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.

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