RecallHawk
Class I Recall

Marketside Fresh Cut Cucumber Slices. In clear deli plastic container with lid. Weights vary. Perishable. Keep Refri

Walmart Inc

Summary

The FDA issued a Class I for Marketside Fresh Cut Cucumber Slices. In clear deli plastic container with lid. by Walmart Inc. Reason: Sliced cucumbers have the potential to be contaminated with Salmonella..

Details

Source

Food Recall

External ID

F-0270-2025

Action Date

2024-12-18

Status

Terminated

Category

food

Product Description

Marketside Fresh Cut Cucumber Slices. In clear deli plastic container with lid. Weights vary. Perishable. Keep Refrigerated. Distributed by Walmart, Inc., Bentonville, AR 72716.

Lot/Code Info: All date codes up to 12/1/2024

Quantity Affected: 650 units

Reason for Recall

Sliced cucumbers have the potential to be contaminated with Salmonella.

Distribution

TX

Type: Voluntary: Firm initiated

Recall Initiated: 2024-11-28

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 63 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 "F-0270-2025" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.

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