CLASS I Food recall · Reported 27 Dec 2023 · FDA Enforcement Report

Mixed Fruit Tray recalled by Kwik Trip

Kwik Trip is recalling Mixed Fruit Tray, distributed in Iowa, Illinois, Michigan, Minnesota, South Dakota, Wisconsin. The recall was initiated on 27 Nov 2023 and the FDA has classified it as Class I.

Check your package

Lot, batch or date codesSell By Date Range: 11/4/2023 - 12/3/2023
Quantity recalled77,013 units total

Do not eat it. Return it to the store for a refund or throw it away. If you have symptoms after eating it, contact a doctor.

Recall details

Recall number
F-0621-2024
FDA event ID
93504
Recalling firm
Kwik Trip, La Crosse, WI
Classification
Class I
Status
Terminated
Recall initiated
27 Nov 2023
FDA classified
16 Dec 2023
Reported
27 Dec 2023
Type
Voluntary: Firm initiated
Customers notified by
Press Release
Reason category
Salmonella
Product category
Other

Timeline

27 Nov 2023Recall initiated by company
16 Dec 2023Classified by FDA+19 days
27 Dec 2023Published in enforcement report+11 days

Companies usually start a recall weeks before the FDA classifies and publishes it; the gap above is that lag.

Reason for recall

Potential Salmonella Contamination.

Salmonella causes fever, diarrhea and abdominal cramps, usually 12 to 72 hours after eating contaminated food. Most people recover without treatment, but severe cases can need hospital care.

Product as listed by the FDA

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

Where it was distributed

IA, IL, MI, MN, SD, and WI

IowaIllinoisMichiganMinnesotaSouth DakotaWisconsin

Questions about this recall

Why was it recalled?

Potential Salmonella Contamination.

Which lots are affected?

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

Where was it sold?

IA, IL, MI, MN, SD, and WI

What should I do if I have it?

Do not eat it. Return it to the store for a refund or throw it away. If you have symptoms after eating it, contact a doctor.

What does Class I mean?

Class I is the most serious FDA recall category: there is a reasonable probability that using the product will cause serious health consequences or death.

Read the official FDA notice · Source record retrieved 26 Sep 2026. The FDA describes openFDA data as unvalidated; the official notice takes precedence. This page reports the record and gives no medical advice.

Other products in this recall event

2 other products · FDA event 93504

This product is part of a recall event; the main page for the event is Mixed Fruit recalled by Kwik Trip.

ReportedClassRecallCompanyReasonWhere
CLASS IMixed Fruit recalled by Kwik TripKwik TripKwik TripSalmonella6 states
CLASS IKwik Trip Cantaloupe, Item recalledKwik TripKwik TripSalmonella6 states

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