Little Leaf Farms brand Southwest Salad Kit; 7.5 oz, clear plastic clamshell; UPC: 857394006220
Summary
The FDA issued a Class I for Little Leaf Farms brand Southwest Salad Kit; 7.5 oz, clear plastic clamshell; UP by LITTLE LEAF FARMS LLC. Reason: Product may contain incorrect salad dressing, resulting in fish and wheat being undeclared..
Details
Source
Food Recall
External ID
F-0637-2025
Action Date
2025-03-19
Status
Terminated
Category
food
Product Description
Little Leaf Farms brand Southwest Salad Kit; 7.5 oz, clear plastic clamshell; UPC: 857394006220
Lot/Code Info: Lot Number: 050011; Enjoy by: 3/08/2025
Quantity Affected: 576 units
Reason for Recall
Product may contain incorrect salad dressing, resulting in fish and wheat being undeclared.
Distribution
MA, NH, CT
Type: Voluntary: Firm initiated
Recall Initiated: 2025-02-28
Company
Shirley, MA
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 55 food recalls issued in the same week, part of 204 food-related FDA actions this month.
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 (LITTLE LEAF FARMS LLC) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.
How often does LITTLE LEAF FARMS LLC have FDA actions?
This is the only FDA action we have on record for LITTLE LEAF FARMS LLC in our database.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "F-0637-2025" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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