Mixed Fruit Products that contain Cantaloupe, Honeydew, and Watermelon, Identified with the following Item ID and Descri
Summary
The FDA issued a Class I for Mixed Fruit Products that contain Cantaloupe, Honeydew, and Watermelon, Identifi by Cut Fruit Express, Inc.. Reason: Cantaloupe containing products may be contaminated with Salmonella..
Details
Source
Food Recall
External ID
F-0588-2024
Action Date
2023-12-20
Status
Terminated
Category
food
Product Description
Mixed Fruit Products that contain Cantaloupe, Honeydew, and Watermelon, Identified with the following Item ID and Description. 4709 Melon Chunk Mix CHW 16 oz.
Lot/Code Info: 11/5/23
Quantity Affected: 2 units
Reason for Recall
Cantaloupe containing products may be contaminated with Salmonella.
Distribution
IL, MN, & WI
Type: Voluntary: Firm initiated
Recall Initiated: 2023-11-24
Company
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 143 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-0588-2024" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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