Food recall

Kwik Trip, Inc. recall: Kwik Trip Cantaloupe

Kwik Trip, Inc., of La Crosse, WI, recalled Kwik Trip Cantaloupe and 2 other products. The FDA's reason: “Potential Salmonella Contamination.” The FDA classified it Class I: it could cause serious harm or death. The company began the recall voluntarily on November 27, 2023, and the FDA first listed it in its Enforcement Report of December 27, 2023. The FDA has closed the recall: it found the company did all it reasonably could to remove or correct the product.

How serious

Class I

It could cause serious harm or death

Why

Salmonella

Status

Terminated

Closed January 11, 2024

The recall

Company
Kwik Trip, Inc. (La Crosse, WI)
Reason, in FDA's words
“Potential Salmonella Contamination.”
Where it was sold
IA, IL, MI, MN, SD, and WI
Recall began
, by the company
FDA classified it
First in an FDA Enforcement Report
FDA event number
93504

The 3 products recalled

As the FDA describes them, with the codes that tell whether a package is part of the recall.

  • F-0619-2024 Class I

    Kwik Trip Cantaloupe, Item 930541. Net Wt 6 oz (170g). UPC 0 39779-00213 7. Produced & Distributed by Kwik Trip Inc., La Crosse WI

    Codes: Sell By Date Range: 11/4/2023 - 12/3/2023

    Quantity: 77,013 units total

  • F-0620-2024 Class I

    Kwik Trip Mixed Fruit, Item 930847. Net Wt 6 oz (170g). UPC 0 39779-00240 3. Produced & Distributed by Kwik Trip Inc., La Crosse WI

    Codes: Sell By Date Range: 11/4/2023 - 12/3/2023

    Quantity: 77,013 units total

  • F-0621-2024 Class I

    Kwik Trip Mixed Fruit Tray, Item 930941. Net Wt 16 oz (1 lb.) 454g. UPC 0 39779-00248 4. Produced & Distributed by Kwik Trip Inc., La Crosse WI

    Codes: Sell By Date Range: 11/4/2023 - 12/3/2023

    Quantity: 77,013 units total

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Source and notes

U.S. Food and Drug Administration, Enforcement Reports (openFDA food recall data) (Public domain (U.S. government work); source U.S. Food and Drug Administration, openFDA), data as of December 27, 2023.

Each week the FDA lists the recalls it has classified in its Enforcement Report, often weeks after the company announced the recall, so a month with five weekly reports tends to count more. Each recall counts once, however many products it covers, in the month FDA first listed it. Class I means the food could cause serious harm or death, Class II temporary or minor harm, and Class III is unlikely to harm anyone. Meat, poultry and most egg products are recalled by the U.S. Department of Agriculture, not the FDA, and aren't included. For what to do with a recalled product, see the FDA's recalls page.