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Recall data is sourced from official U.S. government agencies (CPSC, FDA, NHTSA, USDA) and processed using AI to improve readability. This site is not affiliated with or endorsed by any government agency. Always refer to the original agency notice for authoritative information.

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Critical RiskFDA Food
Food & Beverages/Produce & Fresh

Kwik Trip Fresh Fruit Products Recalled for Potential Salmonella Contamination

Agency Publication Date: December 16, 2023
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Summary

Kwik Trip, Inc. has issued a voluntary recall for approximately 77,013 units of fresh cut fruit products, including Cantaloupe, Mixed Fruit, and Mixed Fruit Trays. The recall was initiated due to potential Salmonella contamination. These products were sold at Kwik Trip and Kwik Star convenience stores across several Midwestern states. No illnesses or injuries have been reported to date in connection with this recall.

Risk

The fruit may be contaminated with Salmonella, which can cause serious and sometimes fatal infections, particularly in children, the elderly, or individuals with weakened immune systems. Healthy people often experience symptoms such as fever, diarrhea, nausea, vomiting, and abdominal pain.

What You Should Do

  1. This recall involves Kwik Trip Cantaloupe (6 oz), Mixed Fruit (6 oz), and Mixed Fruit Trays (16 oz) with 'Sell By' dates between 11/4/2023 and 12/3/2023.
  2. Identify affected products by checking for UPC codes 039779002137 (Cantaloupe), 039779002403 (Mixed Fruit), or 039779002484 (Mixed Fruit Tray) on the product label.
  3. Return the product to any Kwik Trip or Kwik Star store location for a full refund, throw the product away, or contact Kwik Trip, Inc. directly for further instructions.
  4. Call the FDA Consumer Complaint hotline at 1-888-723-3332 for additional information regarding food safety and recalls.

Your Remedy Options

You have 2 options:

💰Option 1: Full Refund
How to: Return the product to the place of purchase for a full refund, or contact the manufacturer or supplier for further instructions
🗑️Option 2: Dispose of Product
How to: Throw the product away.

Affected Products

Product: Kwik Trip Cantaloupe (6 oz)
Item Code:
930541
UPC Codes:
039779002137
Date Ranges: Sell By Date Range: 11/4/2023 - 12/3/2023

Produced & Distributed by Kwik Trip Inc., La Crosse WI

Product: Kwik Trip Mixed Fruit (6 oz)
Item Code:
930847
UPC Codes:
039779002403
Date Ranges: Sell By Date Range: 11/4/2023 - 12/3/2023

Produced & Distributed by Kwik Trip Inc., La Crosse WI

Product: Kwik Trip Mixed Fruit Tray (16 oz)
Item Code:
930941
UPC Codes:
039779002484
Date Ranges: Sell By Date Range: 11/4/2023 - 12/3/2023

Produced & Distributed by Kwik Trip Inc., La Crosse WI

Product Images

Image 1 “Photograph of Mixed Fruit label, 6 oz.”

Image 1 “Photograph of Mixed Fruit label, 6 oz.”

Image 2 “Photograph of Cantaloupe label, 6 oz.”

Image 2 “Photograph of Cantaloupe label, 6 oz.”

Image 3 “Photograph of Fruit Tray label, 16 oz.”

Image 3 “Photograph of Fruit Tray label, 16 oz.”

Additional Information

Agency: Food and Drug Administration (FDA)
Event ID: 93504
Status: Resolved
Manufacturer: Kwik Trip, Inc.
Sold By: Kwik Trip; Kwik Star
Manufactured In: United States
Units Affected: 3 products (77,013 units total)
Distributed To: Iowa, Illinois, Michigan, Minnesota, South Dakota, Wisconsin

Were You Affected by This Recall?

If you or a family member were harmed by this recalled product, you may have legal rights. Consider consulting a consumer protection attorney to understand your options for compensation.

Find an Attorney

This is general information, not legal advice. Go Backs is not a law firm and does not provide legal services.

AI-Enhanced Content: The summary, action steps, and risk assessment on this page were generated by AI from official government recall data to improve readability. This is not legal or medical advice. Always refer to the official agency sources below for authoritative information.

Sources: FDA iRES · FDA Press Release · Raw API Response

openFDA Disclaimer: This recall information is sourced from the openFDA API. Do not rely on openFDA to make decisions regarding medical care. While we make every effort to ensure that data is accurate, you should assume all results are unvalidated. Refer to the openFDA terms of service for more information.