Summary
The FDA issued a Class I for Lettuce in clear plastic 2lb bags. by Fresh Express Incorpated. Reason: The firm was notified by the Florida Department of Agriculture that the products test positive for Listeria monoctyogenes..
Details
Source
Food Recall
External ID
F-0770-2024
Action Date
2024-01-24
Status
Completed
Category
food
Product Description
Lettuce in clear plastic 2lb bags.
Lot/Code Info: G322 Best if use by: DEC-15-23
Quantity Affected: 2,556cs/5/2lb bags
Reason for Recall
The firm was notified by the Florida Department of Agriculture that the products test positive for Listeria monoctyogenes.
Distribution
The product was shipped to the following states: AL, FL, GA, NC, SC, TN & VA.
Type: Voluntary: Firm initiated
Recall Initiated: 2023-12-15
Company
Windermere, FL
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 81 food recalls issued in the same week, part of 204 food-related FDA actions this month.
Fresh Express Incorpated has 9 FDA actions in our database, including 9 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 (Fresh Express Incorpated) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.
How often does Fresh Express Incorpated have FDA actions?
Fresh Express Incorpated has 9 FDA actions in our database, including 9 recalls and 0 device clearances.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "F-0770-2024" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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