CLASS I Food recall · Reported 15 Jan 2025 · FDA Enforcement Report

01035 Cucumber Sliced 5# trays with sealed film recalled

Dairyland Produce is recalling 01035 Cucumber Sliced 5# trays with sealed film, distributed in Texas. The recall was initiated on 27 Nov 2024 and the FDA has classified it as Class I.

Check your package

Lot, batch or date codesX0710777
Quantity recalled4 cases

Do not eat it. Return it to the store for a refund or throw it away. If you have symptoms after eating it, contact a doctor.

Recall details

Recall number
F-0385-2025
FDA event ID
95901
Recalling firm
Dairyland Produce, Houston, TX
Classification
Class I
Status
Terminated
Recall initiated
27 Nov 2024
FDA classified
8 Jan 2025
Reported
15 Jan 2025
Type
Voluntary: Firm initiated
Customers notified by
Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit
Reason category
Salmonella
Product category
Cucumbers

Timeline

27 Nov 2024Recall initiated by company
8 Jan 2025Classified by FDA+42 days
15 Jan 2025Published in enforcement report+7 days

Companies usually start a recall weeks before the FDA classifies and publishes it; the gap above is that lag.

Reason for recall

Cucumbers have the potential to be contaminated with Salmonella.

Salmonella causes fever, diarrhea and abdominal cramps, usually 12 to 72 hours after eating contaminated food. Most people recover without treatment, but severe cases can need hospital care.

Product as listed by the FDA

Texas Harvest Product: 01035 Cucumber Sliced 5# 5-pound trays with sealed film

Where it was distributed

Texas

Texas

Questions about this recall

Why was it recalled?

Cucumbers have the potential to be contaminated with Salmonella.

Which lots are affected?

X0710777

Where was it sold?

Texas

What should I do if I have it?

Do not eat it. Return it to the store for a refund or throw it away. If you have symptoms after eating it, contact a doctor.

What does Class I mean?

Class I is the most serious FDA recall category: there is a reasonable probability that using the product will cause serious health consequences or death.

Read the official FDA notice · Source record retrieved 26 Sep 2026. The FDA describes openFDA data as unvalidated; the official notice takes precedence. This page reports the record and gives no medical advice.

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