RecallHawk
Class I Recall

Caribou Coffee Snack Fruit and Cheese Plate, item # 3818, Net Wt 6.2 oz. (176g) 3 cheeses, red grapes, apples, rosemary

Cut Fruit Express, Inc.

Summary

The FDA issued a Class I for Caribou Coffee Snack Fruit and Cheese Plate, item # 3818, Net Wt 6.2 oz. (176g) by Cut Fruit Express, Inc.. Reason: Brie cheese has the potential to be contaminated with Listeria monocytogenes..

Details

Source

Food Recall

External ID

F-0117-2023

Action Date

2022-11-02

Status

Terminated

Category

food

Product Description

Caribou Coffee Snack Fruit and Cheese Plate, item # 3818, Net Wt 6.2 oz. (176g) 3 cheeses, red grapes, apples, rosemary crackers. Keep Refrigerated. Manufactured By: Cut Fruit Express, Inver Grove Heights, MN

Lot/Code Info: Use By: 9/30/2022, 10/2/2022, 10/4/2022, 10/7/2022 and 10/9/2022

Quantity Affected: 210 units

Reason for Recall

Brie cheese has the potential to be contaminated with Listeria monocytogenes.

Distribution

MN

Type: Voluntary: Firm initiated

Recall Initiated: 2022-10-05

Company

Cut Fruit Express, Inc.

Inver Grove Heights, MN

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 42 food recalls issued in the same week, part of 204 food-related FDA actions this month.

Cut Fruit Express, Inc. has 8 FDA actions in our database, including 8 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 (Cut Fruit Express, Inc.) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.

How often does Cut Fruit Express, Inc. have FDA actions?

Cut Fruit Express, Inc. has 8 FDA actions in our database, including 8 recalls and 0 device clearances.

Where can I find the official FDA record?

The official record is available on FDA.gov. Search for "F-0117-2023" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.

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