Skip to main content

LITTLE LEAF FARMS LLC Recall: Product may contain incorrect salad dressing, resulting in fish and wheat being undeclared.

United States

TerminatedClass I

Company
LITTLE LEAF FARMS LLC
Product
Little Leaf Farms brand Southwest Salad Kit; 7.5 oz, clear p…
Recall date
February 28, 2025
Terminated
April 9, 2025
Source
FDA

Reason for recall

Product may contain incorrect salad dressing, resulting in fish and wheat being undeclared.

  1. - Recall initiated
  2. - Reported by source
  3. - Recall terminated
Recalled products
Product description UPC Quantity Lot / code information
Little Leaf Farms brand Southwest Salad Kit; 7.5 oz, clear plastic clamshell; UPC: 857394006220 857394006220 576 units Lot Number: 050011; Enjoy by: 3/08/2025

Distribution

  • MA
  • NH
  • CT

Official source record

Agency
FDA
Dataset
FDA Food Enforcement (Recalls)
Recall number
F-0637-2025
Event ID
96409
Status
Terminated
Classification
Class I
Company
LITTLE LEAF FARMS LLC
Product description
Little Leaf Farms brand Southwest Salad Kit; 7.5 oz, clear plastic clamshell; UPC: 857394006220
Quantity
576 units
Reason
Product may contain incorrect salad dressing, resulting in fish and wheat being undeclared.
Recall initiation date
February 28, 2025
Report date
March 19, 2025
Classification date
Not published in this source record
Termination date
April 9, 2025
Distribution pattern
MA, NH, CT
UPC, lot, and code information
UPC 857394006220; Lot Number: 050011; Enjoy by: 3/08/2025
Voluntary or mandated
Voluntary: Firm initiated
Initial notification method
Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit
Source last updated
Not tracked separately from the Public Health Trace retrieval date below
Public Health Trace retrieval date

Responsible company: LITTLE LEAF FARMS LLC

Distribution map

A map highlighting the states named in the source's distribution description.

Shading reflects state-level totals only, as published by the source. It does not imply county-level or point-level precision.

Distribution map
State Distributed
Massachusetts 1
New Hampshire 1
Connecticut 1

States shown are extracted from the source's free-text distribution description above; a narrative description (e.g. "distributed nationwide") may not list individual states to extract.

Where this information comes from

View FDA enforcement record -- the specific openFDA record this summary was built from.

No separate FDA public notice was found for this enforcement record. The information below comes from FDA's Recall Enterprise System through openFDA.

FDA Enforcement Reports -- FDA's general, official recall and enforcement information.

Technical source data

View raw source data -- the machine-readable record this page's information was built from.

Retrieved by Public Health Trace:

Frequently asked questions

What does a Class I mean?

A situation in which there is a reasonable probability that use of or exposure to a product will cause serious adverse health consequences or death.

Is this recall still active?

According to FDA, this recall's status is "Terminated." Always confirm the current status using the source links below, since status can change after Public Health Trace last retrieved this record.

What should I do if I have this product?

Follow the instructions published by the responsible agency (see the source links below) -- recall guidance (e.g. dispose of the product, return it for a refund, or check for a specific lot number) varies by recall and is set by that agency, not by Public Health Trace.

Where can I find more official information?

The source links below, published by FDA, are the authoritative record for this recall, including any updates issued after this summary was retrieved.

This summary is based on the official source record referenced above. Public Health Trace does not state that any company or product is unsafe beyond what the official source has published. Read the full medical disclaimer.