Little Salad Bar Cantaloupe Chunks, 1lb clamshell UPC 4099100215885; Market Cuts Cantaloupe Chunk 1" 1/5lb Tray, 5lb tra
Summary
The FDA issued a Class I for Little Salad Bar Cantaloupe Chunks, 1lb clamshell UPC 4099100215885; Market Cuts by Market Cuts LLC. Reason: salmonella.
Details
Source
Food Recall
External ID
F-0609-2024
Action Date
2023-12-13
Status
Terminated
Category
food
Product Description
Little Salad Bar Cantaloupe Chunks, 1lb clamshell UPC 4099100215885; Market Cuts Cantaloupe Chunk 1" 1/5lb Tray, 5lb tray; Market Cuts1 lb Cantaloupe Chunk 1"x1", 1lb clamshell UPC 092538001277; Market Cuts Cantaloupe Chunk 1" 2/5lb Tray, 5lb tray; Market Cuts Cantaloupe Chunk 3/4" 2/5lb Tray, 5lb tray; Market Cuts Cantaloupe Chunk 3/4" 1/5lb Tray, 5lb tray; (No brand) 10 oz Cantaloupe Chunk Grab n Go, 10oz cup UPC 092538002038; (No brand) 1 lb Cantaloupe Chunk 1"x1", 1lb tray UPC 092538001277; Market Cuts 6 oz Cantaloupe Chunk Grab n Go, 6oz cup UPC 092538002762
Lot/Code Info: Best By 11/4/2023 to 11/9/2023
Quantity Affected: 4240 individual units
Reason for Recall
salmonella
Distribution
IL, IN, MI, WI
Type: Voluntary: Firm initiated
Recall Initiated: 2023-11-09
Company
Chicago, IL
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 56 food recalls issued in the same week, part of 204 food-related FDA actions this month.
Market Cuts LLC 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 (Market Cuts LLC) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.
How often does Market Cuts LLC have FDA actions?
Market Cuts LLC 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-0609-2024" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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