RecallHawk
Class I Recall

Cucumbers, Wholesale Produce Supply, 752 Kasota Circle, Minneapolis, MN 554145. Product of Mexico. Cucumbers sold in t

WHOLESALE PRODUCE SUPPLY LLC DBA

Summary

The FDA issued a Class I for Cucumbers, Wholesale Produce Supply, 752 Kasota Circle, Minneapolis, MN 554145. by WHOLESALE PRODUCE SUPPLY LLC DBA. Reason: Cucumbers may be contaminated with Salmonella..

Details

Source

Food Recall

External ID

F-0400-2025

Action Date

2025-01-22

Status

Terminated

Category

food

Product Description

Cucumbers, Wholesale Produce Supply, 752 Kasota Circle, Minneapolis, MN 554145. Product of Mexico. Cucumbers sold in the following pack sizes: 1. 5 lb. pack 2. 6 ct individual items per case. 3. 12 ct individual items per case. 4. 24 ct individual items per case. 5. 36 ct individual items per case.

Lot/Code Info: Pack Date: 79 24353 Lot 542547

Quantity Affected: 1178 units

Reason for Recall

Cucumbers may be contaminated with Salmonella.

Distribution

IA, IL, KS, MN, MT, ND, NE, SD, WI and Canada

Type: Voluntary: Firm initiated

Recall Initiated: 2024-12-12

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 29 food recalls issued in the same week, part of 204 food-related FDA actions this month.

WHOLESALE PRODUCE SUPPLY LLC DBA has 12 FDA actions in our database, including 12 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 (WHOLESALE PRODUCE SUPPLY LLC DBA) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.

How often does WHOLESALE PRODUCE SUPPLY LLC DBA have FDA actions?

WHOLESALE PRODUCE SUPPLY LLC DBA has 12 FDA actions in our database, including 12 recalls and 0 device clearances.

Where can I find the official FDA record?

The official record is available on FDA.gov. Search for "F-0400-2025" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.

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