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Dairyland Produce, LLC Recall: Cucumbers have the potential to be contaminated with Salmonella.

United States

TerminatedClass I

Company
Dairyland Produce, LLC
Product
Texas Harvest Product: 01035 Cucumber Sliced 5# 5-pound tray…
Recall date
November 27, 2024
Terminated
February 11, 2025
Source
FDA

Reason for recall

Cucumbers have the potential to be contaminated with Salmonella.

  1. - Recall initiated
  2. - Reported by source
  3. - Recall terminated
Recalled products
Product description UPC Quantity Lot / code information
Texas Harvest Product: 01035 Cucumber Sliced 5# 5-pound trays with sealed film Not published in this source record 4 cases X0710777

Distribution

  • Texas

Official source record

Agency
FDA
Dataset
FDA Food Enforcement (Recalls)
Recall number
F-0385-2025
Event ID
95901
Status
Terminated
Classification
Class I
Company
Dairyland Produce, LLC
Product description
Texas Harvest Product: 01035 Cucumber Sliced 5# 5-pound trays with sealed film
Quantity
4 cases
Reason
Cucumbers have the potential to be contaminated with Salmonella.
Recall initiation date
November 27, 2024
Report date
January 15, 2025
Classification date
Not published in this source record
Termination date
February 11, 2025
Distribution pattern
Texas
UPC, lot, and code information
X0710777
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: Dairyland Produce, LLC

Other recalls from Dairyland Produce, LLC

FDA Recall United States Ongoing 2026 recordClass I

Dairyland Produce, LLC

Product
Dairyland Produce, LLC Pepper Jalapeno, repackaged into the…
Published
August 26, 2026
Distribution
LA and TX

View recall →

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.