Cut Fresh Luau Blend Fruit Mix "F&F". 4/10 oz. Fresh & Finest. Contains: Cantaloupe, Honeydew, Pineapple, Red Grapes
Summary
The FDA issued a Class I for Cut Fresh Luau Blend Fruit Mix "F&F". 4/10 oz. Fresh & Finest. Contains: Can by WHOLESALE PRODUCE SUPPLY LLC DBA. Reason: Potential Listeria monocytogenes contamination..
Details
Source
Food Recall
External ID
H-0063-2026
Action Date
2025-10-22
Status
Terminated
Category
food
Product Description
Cut Fresh Luau Blend Fruit Mix "F&F". 4/10 oz. Fresh & Finest. Contains: Cantaloupe, Honeydew, Pineapple, Red Grapes, Strawberry, Blueberry. Keep Refrigerated. UPC 0 70253-00572 5. Packed by WPS, Minneapolois, MN
Lot/Code Info: Lot Number: X0924878 Expiration 10/4/2025.
Quantity Affected: 307 total cases/pails recalled
Reason for Recall
Potential Listeria monocytogenes contamination.
Distribution
IA, IL, ND, NE, WI
Type: Voluntary: Firm initiated
Recall Initiated: 2025-09-26
Company
Minneapolis, MN
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 75 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 "H-0063-2026" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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