Cut Fresh Fruit Mix. Contains: Cantaloupe, Honeydew

WHOLESALE PRODUCE SUPPLY LLC DBA has recalled Cut Fresh Fruit Mix. Contains: Cantaloupe, Honeydew, according to data published by the U.S. Food and Drug Administration (FDA). The recall was reported on October 22, 2025 and was initiated on September 26, 2025. It is classified as a Class I recall, which means there is a reasonable chance that using this product could cause serious health problems or death.

Below is a plain-English summary of what was recalled, why it was recalled, how to tell whether you have the affected product, and what steps you can take. For the complete and most current details, you can view the FDA record linked further down this page.

What was recalled?

This recall covers Cut Fresh Fruit Mix. Contains: Cantaloupe, Honeydew, with approximately 307 total cases/pails recalled affected. The company behind the recall is WHOLESALE PRODUCE SUPPLY LLC DBA, based in Minneapolis, MN. The FDA describes the product as: “Cut Fresh Fruit Mix. Contains: Cantaloupe, Honeydew, and Red Grapes. Keep Refrigerated. Packed under the following brands and sizes: 1. Fruit Mix "HC" 6/6oz. UPC 7 90629-11821 6. 2. Fruit Medley "F&F" 4/12 oz. Fresh & Finest UPC 0 70253-00573 2 3. Fruit Mix 4…”

Why was Cut Fresh Fruit Mix. Contains: Cantaloupe, Honeydew recalled?

According to the FDA, the stated reason for the recall is: “Potential Listeria monocytogenes contamination.” In plain terms, this recall relates to Listeria.

Listeria monocytogenes is a bacterium that can grow even at refrigerator temperatures, which makes it a particular concern in ready-to-eat foods. Health authorities warn that it can cause a serious infection called listeriosis, and that pregnant people, newborns, older adults, and those with weakened immune systems are especially vulnerable. This is why products potentially contaminated with Listeria are often recalled quickly.

What should you do?

If you think you may have bought Cut Fresh Fruit Mix. Contains: Cantaloupe, Honeydew, compare it against the product description and identifying codes (1. Lot Number: X0924913, Expiration 10/4/2025, and Lot Number: X0925463, Expiration 10/4/2025. 2. Lot Number: X0924882, Expiration 10/4/2025. 3. Lot Number: X0…) before using it.

The general guidance for a matching product is to stop using it and follow the instructions in the official FDA recall notice, which may include a repair, replacement, refund, or safe disposal. When in doubt, contact WHOLESALE PRODUCE SUPPLY LLC DBA or your local health authority.

About this recall

This recall was distributed in MN. RecallRadar summarizes recall information from public FDA data to make it easier to understand. We are an independent service and are not affiliated with the FDA or any government agency, so please always refer to the official source for the authoritative record — and note the “last synced” date shown on this page, since recall details can change over time.