CLASS I Food recall · Reported 22 Oct 2025 · FDA Enforcement Report

Cut Fresh Cantaloupe Chunks packaged into the following recalled

Wholesale Produce Supply is recalling Cut Fresh Cantaloupe Chunks packaged into the following size containers some under, distributed in Iowa, Illinois, North Dakota, Nebraska, Wisconsin. The recall was initiated on 26 Sep 2025 and the FDA has classified it as Class I.

Check your package

Lot, batch or date codesLot 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
Quantity recalled307 total cases/pails recalled

Do not eat it. Return it to the store for a refund or throw it away. If you have symptoms after eating it, contact a doctor.

Recall details

Recall number
H-0059-2026
FDA event ID
97709
Recalling firm
Wholesale Produce Supply, Minneapolis, MN
Brand
Cut
Classification
Class I
Status
Terminated
Recall initiated
26 Sep 2025
FDA classified
15 Oct 2025
Reported
22 Oct 2025
Type
Voluntary: Firm initiated
Customers notified by
E-Mail
Reason category
Listeria
Product category
Melons

Timeline

26 Sep 2025Recall initiated by company
15 Oct 2025Classified by FDA+19 days
22 Oct 2025Published in enforcement report+7 days

Companies usually start a recall weeks before the FDA classifies and publishes it; the gap above is that lag.

Reason for recall

Potential Listeria monocytogenes contamination.

Listeria monocytogenes can grow at refrigerator temperatures. Infection is most dangerous for pregnant women, newborns, older adults and people with weakened immune systems. Symptoms can appear up to 70 days after eating contaminated food.

Product as listed by the FDA

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

Where it was distributed

IA, IL, ND, NE, WI

IowaIllinoisNorth DakotaNebraskaWisconsin

Questions about this recall

Is Cut Fresh Cantaloupe Chunks packaged into the following size containers some under recalled?

Yes. Wholesale Produce Supply recalled Cut Fresh Cantaloupe Chunks packaged into the following size containers some under on 26 Sep 2025. The recall is Class I and its status is Terminated. Recall number H-0059-2026.

Why was it recalled?

Potential Listeria monocytogenes contamination.

Which lots are affected?

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

Where was it sold?

IA, IL, ND, NE, WI

What should I do if I have it?

Do not eat it. Return it to the store for a refund or throw it away. If you have symptoms after eating it, contact a doctor.

What does Class I mean?

Class I is the most serious FDA recall category: there is a reasonable probability that using the product will cause serious health consequences or death.

Read the official FDA notice · Source record retrieved 21 Sep 2026. The FDA describes openFDA data as unvalidated; the official notice takes precedence. This page reports the record and gives no medical advice.

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