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Food FDA Class I Terminated Pathogen contamination

Cut Fresh Fruit Mix. Contains: Cantaloupe, Honeydew, Watermelon and Red Grapes. Keep Refrigerated. Packed under the following brands and sizes: 1. Fruit Mix CHWG (MCT) 1/5 lb. UPC 7 90629-11173 6. 2. Melon Mix Bowl & Grapes "HC" 2/48 oz. Harvest Cuts UPC 7 90629-10225 3. Packed by WPS,

WHOLESALE PRODUCE SUPPLY LLC DBA Published Oct 22, 2025

Risk level

Class I

Dangerous or defective — could cause serious health problems or death.

Severity score 95/100

What should you do?

  • Check whether you have this product, using the lot codes, UPCs, and dates listed below.
  • Do not eat, serve, or sell the affected product.
  • Return it to the place of purchase for a refund, or throw it away in a sealed bag so people and animals can’t get to it.
  • Contact WHOLESALE PRODUCE SUPPLY LLC DBA or your place of purchase with questions, and see the source record below for full details.
Reason for recall

Potential Listeria monocytogenes contamination.

Hazards

Listeria monocytogenes · primary

Affected products (1)

Cut Fresh Fruit Mix. Contains: Cantaloupe, Honeydew, Watermelon and Red Grapes. Keep Refrigerated. Packed under the following brands and sizes: 1. Fruit Mix CHWG (MCT) 1/5 lb. UPC 7 90629-11173 6. 2. Melon Mix Bowl & Grapes "HC" 2/48 oz. Harvest Cuts UPC 7 90629-10225 3. Packed by WPS, Minneapolois, MN

307 total cases/pails recalled

Lot codes: Number
Code info: 1. Lot Number: X0924993, Expiration 10/5/2025. 2. Lot Number: X0924935, Expiration 10/4/2025 and Lot Number: X0925460, Expiration 10/4/2025.

Affected areas

IllinoisIowaNebraskaNorth DakotaWisconsin

Timeline

  1. Initiated
    Sep 26, 2025
  2. Published
    Oct 22, 2025
  3. Terminated
    Dec 19, 2025
Recall number
H-0066-2026
Agency
U.S. Food and Drug Administration
Country
US
Source data (openFDA JSON) About FDA enforcement reports

FDA records come from the openFDA food enforcement-report dataset — the agency's full weekly enforcement list. Most entries are not issued as consumer press releases, so they won't appear on fda.gov/recalls or in a web search. The source record link above resolves this exact recall by its number.