← FDA ENFORCEMENT
F-0619-2024Class I

Kwik Trip, Inc.

What this record is not

A recall record is reproduced as FDA published it, and the classification is FDA’s. SPEQ adds no interpretation, and a recall concerns the products and dates in the record — it is not a statement about a company’s other products or its current status.

Recalling firm
Kwik Trip, Inc.
Product type
Food / supplement / cosmetic
Status
Terminated
Report date
2023-12-27
Distribution
IA, IL, MI, MN, SD, and WI
Firm state
WI
Product quantity
77,013 units total
Initiated by
Voluntary: Firm initiated
SPEQ quality domain
Environmental Monitoring
Reason for recall

Potential Salmonella Contamination.

Product description

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

Code / lot info

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

Other recalls SPEQ maps to Environmental Monitoring
See all Environmental Monitoring recalls →

Data: U.S. FDA. Recall details are as reported by the FDA. The quality-domain mapping and severity are a SPEQ editorial interpretation of the recall reason, not an official FDA classification. Open the enforcement explorer →