Trader Joe's Fresh Cut Fruit Cantaloupe Chunks NET WT 16 OZ (1 LB) 453g UPC 0095 2668, DIST & SOLD EXCLUSIVELY BY TRADER
Summary
The FDA issued a Class I for Trader Joe's Fresh Cut Fruit Cantaloupe Chunks NET WT 16 OZ (1 LB) 453g UPC 0095 by Renaissance Food Group. Reason: Salmonella.
Details
Source
Food Recall
External ID
F-0637-2024
Action Date
2023-12-27
Status
Terminated
Category
food
Product Description
Trader Joe's Fresh Cut Fruit Cantaloupe Chunks NET WT 16 OZ (1 LB) 453g UPC 0095 2668, DIST & SOLD EXCLUSIVELY BY TRADER JOE'S MONROVIA, CA 91016
Lot/Code Info: SELL BY 11/1/2023, GHGA 297, SELL BY 11/2/2023, GHGA 298, SELL BY 11/7/2020, GHGA 303, SELL BY 11/8/2023, GHGA 304
Quantity Affected: 175cs/12/1lb pkgs = 2100 units
Reason for Recall
Salmonella
Distribution
Product was shipped to the following states: AL, GA, FL, NC, SC
Type: Voluntary: Firm initiated
Recall Initiated: 2023-11-24
Company
Conley, GA
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.
Renaissance Food Group has 40 FDA actions in our database, including 40 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 (Renaissance Food Group) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.
How often does Renaissance Food Group have FDA actions?
Renaissance Food Group has 40 FDA actions in our database, including 40 recalls and 0 device clearances.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "F-0637-2024" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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