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