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H-0059-2026Class I

WHOLESALE PRODUCE SUPPLY LLC DBA

What this record is not

A recall record is reproduced as FDA published it, and the classification is FDA’s. SPEQ adds no interpretation, and a recall concerns the products and dates in the record — it is not a statement about a company’s other products or its current status.

Recalling firm
WHOLESALE PRODUCE SUPPLY LLC DBA
Product type
Food / supplement / cosmetic
Status
Terminated
Report date
2025-10-22
Distribution
IA, IL, ND, NE, WI
Firm state
MN
Product quantity
307 total cases/pails recalled
Initiated by
Voluntary: Firm initiated
SPEQ quality domain
Environmental Monitoring
Reason for recall

Potential Listeria monocytogenes contamination.

Product description

Cut Fresh Cantaloupe Chunks packaged into the following size containers some under brand names Fresh & Finest or Harvest Cuts: 1. CANTALOUPE CHUNKS "PRMK" 30/2 OZ 2. CANTALOUPE CHUNKS "HC" 6/6 OZ. Harvest Cuts UPC 7 90629-11820 9. 3. CANTALOUPE CHUNKS "HC" 24/8 OZ. Harvest Cuts UPC 7 90629-09780 1. 4. CANTALOUPE CHUNKS "F&F" 4/12 OZ. Fresh & Finest UPC 0 70253-00583 1. 5. CANTALOUPE SPEARS "HC" 4/16 OZ. Harvest Cuts UPC 7 90629-11929 9. 6. CANTALOUPE CHUNKS "HC" 4/16 OZ. Harvest Cuts UPC 7 90629-08002 5. 7. CANTALOUPE CHUNKS 4/28 OZ 8. CANTALOUPE CHUNKS (MCT) MC 1/5 LB. and 4/5 LB. UPC 7 90629-06408 7. 9. Cantaloupe Chunks (MCT) "PRMK" 1/5lb. Keep Refrigerated. Packed by WPS, Minneapolois, MN

Code / lot info

Lot Number: 1. X0925047 Expiration 10/5/2025. 2. X0924912, and X0925451 Expiration 10/4/2025. 3. X0925248 Expiration 10/4/2025. 4. X0924879 Expiration 10/4/2025. 5. X0924922 and X0925452 Expiration 10/4/2025. 6. X0924921 and X0925450 Expiration 10/4/2025. 7. X0925449 Expiration 10/4/2025. 8. Lot Numbers: X0924979, X0924980, X0924982, X0924982, X0925155, X0924981. Expiration 10/5/2025. 9. 1/5 lb. Lot Number: X0924982. 4/5 lb. Lot Number: X0924981. Expiration 10/5/2025

Data: U.S. FDA. Recall details are as reported by the FDA. The quality-domain mapping and severity are a SPEQ editorial interpretation of the recall reason, not an official FDA classification. Open the enforcement explorer →