RecallHawk
Class I Recall

Fresh cut cucumber slices, Marketside, packaged in clear plastic circular container with clear plastic lid and white adh

Walmart Inc

Summary

The FDA issued a Class I for Fresh cut cucumber slices, Marketside, packaged in clear plastic circular contai by Walmart Inc. Reason: Potential Salmonella contamination..

Details

Source

Food Recall

External ID

H-0003-2025

Action Date

2025-06-11

Status

Terminated

Category

food

Product Description

Fresh cut cucumber slices, Marketside, packaged in clear plastic circular container with clear plastic lid and white adhesive label with black print, Walmart, Inc. Bentonville, AR 72716

Lot/Code Info: 00262969000006., all date codes up to 5/24/25

Quantity Affected: 522 units based on point of sale information at stores

Reason for Recall

Potential Salmonella contamination.

Distribution

12 Retail locations in Texas: Ennis, TX; Palestine, TX; Longview, TX; Benbrook/Ft. Worth, TX; Wichita Falls, TX; Frisco Stonebrook, TX; Longview (SE), TX; Saginaw, TX; Rockwall, TX; Lindale, TX; Irving, TX; Paris, TX

Type: Voluntary: Firm initiated

Recall Initiated: 2025-05-20

Company

Walmart Inc

Bentonville, AR

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 123 food recalls issued in the same week, part of 204 food-related FDA actions this month.

Walmart Inc has 7 FDA actions in our database, including 7 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 (Walmart Inc) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.

How often does Walmart Inc have FDA actions?

Walmart Inc has 7 FDA actions in our database, including 7 recalls and 0 device clearances.

Where can I find the official FDA record?

The official record is available on FDA.gov. Search for "H-0003-2025" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.

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