RecallHawk
Class I Recall

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

Kwik Trip, Inc.

Summary

The FDA issued a Class I for Kwik Trip Mixed Fruit Tray, Item 930941. Net Wt 16 oz (1 lb.) 454g. UPC 0 3977 by Kwik Trip, Inc.. Reason: Potential Salmonella Contamination..

Details

Source

Food Recall

External ID

F-0621-2024

Action Date

2023-12-27

Status

Terminated

Category

food

Product Description

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

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

Quantity Affected: 77,013 units total

Reason for Recall

Potential Salmonella Contamination.

Distribution

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

Type: Voluntary: Firm initiated

Recall Initiated: 2023-11-27

Company

Kwik Trip, Inc.

La Crosse, WI

Context & Analysis

This is a Class I recall. Class I recalls are the most serious — there is a reasonable probability that use of or exposure to the product will cause serious health consequences or death.

This was one of 157 food recalls issued in the same week, part of 204 food-related FDA actions this month.

Kwik Trip, Inc. has 3 FDA actions in our database, including 3 recalls.

Frequently Asked Questions

What is a Class I recall?

A Class I recall is the most serious type. The FDA has determined there is a reasonable probability that the product will cause serious adverse health consequences or death. Consumers should stop using the product immediately.

What should I do if I have this product?

Stop using the product. Check the product against the specific lot numbers or identifiers listed in the recall. Contact the manufacturer (Kwik Trip, Inc.) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.

How often does Kwik Trip, Inc. have FDA actions?

Kwik Trip, Inc. has 3 FDA actions in our database, including 3 recalls and 0 device clearances.

Where can I find the official FDA record?

The official record is available on FDA.gov. Search for "F-0621-2024" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.

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