The Recall Desk
Agency classClass IOur severity:SevereFDA (Food)·F-0619-2024·Announced 2023-12-27

Kwik Trip Cantaloupe Recalled for Potential Salmonella Contamination

Kwik Trip Cantaloupe (Item 930541, 6 oz) is being recalled due to potential Salmonella contamination. Affected products were distributed in Iowa, Illinois, Michigan, Minnesota, South Dakota, and Wisconsin with sell-by dates from November 4 to December 3, 2023.

The agency’s classification

FDA (Food): Class I

Class I is a situation in which there is a reasonable probability that the use of or exposure to a violative product will cause serious adverse health consequences or death.

This is the agency’s own classification, taken from its notice. The severity score below is our assessment, not the agency’s. How recall classes work

What this means for you

Our assessment, not the agency’s: severity 4/5 (Severe).

The hazard poses a serious risk of illness, injury, or structural failure. Stop using the product immediately and contact the manufacturer for a refund or repair.

Our severity reasoning: FDA Class I classification requires a minimum severity score of 4. Salmonella is a high-risk pathogen with potential for foodborne illness.

Plain-English summary

Kwik Trip, Inc., La Crosse, Wisconsin, is recalling approximately 77,013 units of Kwik Trip Cantaloupe (Item 930541, 6 oz / 170g, UPC 0 39779-00213 7) due to potential Salmonella contamination.

Salmonella is a bacterium that may cause foodborne illness. The FDA issued this Class I recall to protect public health.

The recalled cantaloupe was distributed to retail locations in Iowa, Illinois, Michigan, Minnesota, South Dakota, and Wisconsin. Products bearing sell-by dates from November 4, 2023 to December 3, 2023 are included in this recall.

Consumers should not consume the recalled cantaloupe. Those who have purchased this product are advised to return it to the point of purchase or dispose of it.

The recalled product

Product
Kwik Trip Cantaloupe, Item 930541. Net Wt 6 oz (170g). UPC 0 39779-00213 7. Produced & Distributed by Kwik Trip Inc., La Crosse WI
Manufacturer
Kwik Trip, Inc.
Affected units
77,013

Is your product affected?

Check your packaging against the codes below. If any of them match, the product is part of this recall.

Lot numbers (1)

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

Distribution

Distributed in 6 states:

Part of a larger recall action

This product is one of 3 recalled by Kwik Trip, Inc. under a single FDA (Food) recall action. The agency files each product separately, so the size of the action is not visible from this page alone.

See all 3 products in this recall →

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